Future FinTech and China Foundation of Consumer Protection Enter Into Cooperation Agreement to Use Blockchain Technology Against Counterfeit Products

PR Newswire

NEW YORK, Feb. 12, 2021 /PRNewswire/ — Future FinTech Group Inc. (NASDAQ: FTFT) (“Future FinTech”, “FTFT” or “Company”), a leading blockchain based e-commerce business and a fintech service provider, announced today that, its wholly-owned subsidiary Chain Cloud Mall Network and Technology (Tianjin) Co., Limited (“CCM”) has signed a cooperation agreement with The Merchandise and Quality Week Magazine, a news magazine directly owned by China Foundation of Consumer Protection. The cooperation has a term for five years, from February 1, 2021 to January 31, 2026. The Anti-Counterfeiting Committee of China Foundation of Consumer Protection will set up a “Quality and Safety Office” and appoint Mr. Zhi Yan, the general manager of CCM, as the deputy director of that office for a term of one year, who will be responsible for building the quality and safety credit system for Chinese brands and enterprises under the “Responsible Brand Plan”. The “Responsible Brand Plan” will be officially launched in March 2021 and operated by the “Quality and Safety Office” of the Anti-Counterfeiting Committee of China Foundation of Consumer Protection.

Mr. Zhi Yan said that: “The Responsible Brand Plan will make full use of the real name based blockchain anti-counterfeiting tracing technology developed by CCM, which will not only protect the legitimate rights and interests of the enterprises and their brands, but also impose  responsibility for their product’s quality and safety.”

China Foundation of Consumer Protection was established in November 1989. It is supervised by the State Owned Assets Supervision and Administration Commission of the State Council of China. Its mission is to protect the interest of consumers and implement its responsibility as a nonprofit consumer protection organization under the Consumer Protection Law of China. One of its main responsibilities is to support and participate in anti-counterfeiting activities and clean up the consumer products market.

The Anti-Counterfeiting Committee of China Foundation of Consumer Protection is the first and the only nonprofit organization that was approved by the Ministry of Civil Affairs specializing in anti-counterfeiting in China. It was established in July 2000. It focuses on cracking down counterfeit and shoddy products that harm the rights and interest of consumers.

About Future FinTech Group Inc.

Future FinTech Group Inc. (“Future FinTech”, “FTFT” or the “Company”) is a leading blockchain e-commerce company and a service provider for financial technology incorporated in Florida. The Company’s operations include a blockchain-based online shopping mall platform, Chain Cloud Mall (“CCM”), a cross-border e-commerce platform (NONOGIRL), an incubator for blockchain based application projects. The Company is also engaged in the development of blockchain based technology and services as well as financial technology services. For more information, please visit http://www.ftftex.com/.

Safe Harbor Statement 

Certain of the statements made in this press release are “forward-looking statements” within the meaning and protections of Section 27A of the Securities Act of 1933, as amended and Section 21E of the Securities Exchange Act of 1934, as amended, or the Exchange Act. Forward-looking statements include statements with respect to our beliefs, plans, objectives, goals, expectations, anticipations, assumptions, estimates, intentions, and future performance, and involve known and unknown risks, uncertainties and other factors, which may be beyond our control, and which may cause the actual results, performance, capital, ownership or achievements of the Company to be materially different from future results, performance or achievements expressed or implied by such forward-looking statements. All statements other than statements of historical fact are statements that could be forward-looking statements. You can identify these forward-looking statements through our use of words such as “may,” “will,” “anticipate,” “assume,” “should,” “indicate,” “would,” “believe,” “contemplate,” “expect,” “estimate,” “continue,” “plan,” “point to,” “project,” “could,” “intend,” “target” and other similar words and expressions of the future.

All written or oral forward-looking statements attributable to us are expressly qualified in their entirety by this cautionary notice, including, without limitation, those risks and uncertainties described in our annual report on Form 10-K for the year ended December 31, 2019 and our other reports and filings with SEC. Such reports are available upon request from the Company, or from the Securities and Exchange Commission, including through the SEC’s Internet website at http://www.sec.gov. We have no obligation and do not undertake to update, revise or correct any of the forward-looking statements after the date hereof, or after the respective dates on which any such statements otherwise are made.

 

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SOURCE Future FinTech Group Inc.

REPLY: Airwalk Reply Achieves AWS Financial Services Competency Status

REPLY: Airwalk Reply Achieves AWS Financial Services Competency Status

TURIN, Italy–(BUSINESS WIRE)–
Airwalk Reply, specialized in the design and delivery of cloud based services and solutions for Financial Services, Government and the Public Sector, announced today that it has achieved Amazon Web Services (AWS) Financial Services Competency status. This designation recognizes Airwalk Reply for providing deep expertise to help organizations manage critical issues pertaining to the industry, such as risk management, core systems implementations, data management, navigating compliance requirements, and establishing governance models.

Achieving the AWS Financial Services Competency differentiates Airwalk Reply as AWS Partner Network (APN) member has demonstrated relevant technical proficiency and proven customer success, delivering solutions seamlessly on AWS. To receive the designation, APN Partners must possess deep AWS expertise and undergo an assessment of the security, performance, and reliability of their solutions.

Filippo Rizzante, CTO Reply, commented: “We are proud to have achieved this competency. Airwalk Reply is dedicated to helping customers in the financial services industry achieve their business goals by leveraging the agility of AWS and attainment of this competency designation will help us to offer our services to an even bigger group of customers in the UK and South East Asia where they operate”.

Airwalk Reply delivers transformation change in complex, highly regulated environments and brings together experienced multi-disciplined teams with business and technical knowledge and expertise and solutions to support customers specifically in the Financial Services Industry.

AWS is enabling scalable, flexible, and cost-effective solutions from start-ups to global enterprises. To support the seamless integration and deployment of these solutions, AWS established the AWS Competency Program to help customers identify Consulting and Technology APN Partners with deep industry experience and expertise.

As an APN Premier Consulting Partner, Airwalk Reply helps customer to digitally transform by building innovative solutions powered by AWS services.

Airwalk Reply

Airwalk Reply is the Reply group company specialised in the design and delivery of cloud based services and solutions, driving technology-led transformational change in complex, regulated industries such as Financial Services, Government and the Public Sector. We bring a unique combination of deep technical subject matter expertise across technology strategy, architecture, service design, engineering and security, alongside business domain expertise and a heavyweight delivery capability. www.airwalkreply.com

Media

Reply

Fabio Zappelli

[email protected]

Tel. +390117711594

Aaron Miani

[email protected]

Tel. +44 (0)20 7730 6000

KEYWORDS: Italy Europe

INDUSTRY KEYWORDS: Technology Finance Consulting Other Technology Telecommunications Professional Services Software Networks Internet Data Management

MEDIA:

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Bambuser Expands Live Video Shopping Production Capabilities for with Launch of Dual Hosting & External Camera Compatibility

Latest platform developments bring retailers greater flexibility and control over creation and delivery of interactive e-commerce experiences

PR Newswire

STOCKHOLM, Feb. 12, 2021 /PRNewswire/ — Bambuser today announced the launch of new dual host broadcasting capabilities and compatibility with external cameras and software, two in-demand features that give brands and retailers greater flexibility and control over their Live Video Shopping productions. The product updates closely follow several other major platform enhancements released to help customers increase awareness of and drive traffic to their interactive e-commerce initiatives. 

Dual Hosting for Split Screen Broadcasting

Bambuser’s Dual Hosting solves production challenges posed by stay-at-home recommendations and social distancing requirements, enabling Live Video Shopping events to have hosts and guests in different locations. As part of the Broadcaster app for iOS, Dual Hosting enables brands and retailers to easily produce shows featuring different hosts, guests and other influencers, each from a different location. The platform currently supports two simultaneous connections without lag, quality degradation or interruption to the platform’s e-commerce functionality. 

During extensive beta testing, Bambuser observed lifts in viewer engagement metrics such as the quantity of activities in the live chat during shows that leveraged dual hosting. The company attributes this improved performance to the more immersive and conversational nature of the split screen, dual host experience. 

Bambuser’s dual host broadcasting is currently in final testing and will be rolling out broadly within the next couple of months. To see how the dual host streaming works, check out this video: http://bmb.sr/dual

External Camera Compatibility

Expanding on the platform’s extensive mobile capabilities, Bambuser now supports the use of external hardware and software in show production. By leveraging Real-Time Messaging Protocol (RTMP), Bambuser now provides brands and retailers with more opportunities to create shows using the cameras and other tools of their choosing. With this added flexibility, they have more opportunity to deliver unique experiences and polished programs in line with their brands.

“Every day, our development team focuses on anticipating the needs of our customers as well as our customers’ customers. We’re incredibly proud to announce dual hosting and external camera compatibility, as we believe these features deliver benefit to both those groups,” said Jesper Funck, Chief Product Officer at Bambuser. For our retail and brand partners, we’re giving more power to customize the format and production quality of their shows. For their customers who participate in Live Video Shopping, we’re offering more engaging and interactive experiences that are consistently the highest quality possible.”

A pioneer in live video streaming since inception in 2007, Bambuser is pursuing an aggressive product development strategy to ensure the platform remains the most feature rich and robust available. The company is leveraging the recent investment of $60 million from renowned fashion and technology investor Anders Holch Povlsen along with Lancelot Asset Management AB, TIN Fonder and Handelsbanken Fonder, to accelerate its timeline for rolling out new capabilities. 

Contact information

Maryam Ghahremani

CEO Bambuser
[email protected] 
+46 8 400 160 02

About Bambuser

Bambuser is a software company specializing in interactive live video streaming. The Company’s primary product, Live Video Shopping, is a cloud-based software solution that is used by customers such as global e-commerce and retail businesses to host live shopping experiences on websites, mobile apps and social media. Bambuser was founded in 2007 and has its headquarters in Stockholm. Erik Penser Bank AB is Bambuser’s Certified Adviser.

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https://news.cision.com/bambuser/r/bambuser-expands-live-video-shopping-production-capabilities-for-with-launch-of-dual-hosting—exter,c3285804

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SOURCE Bambuser

Sosei Heptares Operational Highlights and Consolidated Results for the 12 Months ended 31 December 2020

PR Newswire

TOKYO and CAMBRIDGE, England, Feb. 12, 2021 /PRNewswire/ — Sosei Group Corporation (“the Company”) (TSE: 4565) provides an update on operational activities and reports its consolidated results for the 12 months ended 31 December 2020. The full report can be accessed by clicking here


Shinichi Tamura, Chairman, President and CEO of Sosei Heptares, commented:
 “Sosei Heptares made a great deal of progress across all areas of its business in 2020, despite the challenges we faced. We adapted extremely well to the COVID-19 pandemic. This allowed us to successfully execute our strategy, adding several major partnering agreements around our early-stage programs, reinforcing our position as a leading go-to drug discovery and development partner. We also entered several strategic technology collaborations with innovative companies designed to strengthen our StaR® technology and SBDD capabilities and enhance our discovery and future partnering opportunities, including beyond GPCRs. In addition, we successfully refinanced the business, which is supporting the rapid advancement of our exciting and extensive pipeline and our ambitious growth plans, which could include a potentially transformative acquisition. Our ability to deliver further partnering and/or co-investment deals was further enhanced when we regained the rights to our muscarinic program early in the new year. With our clear strategy, our talented team and a strong financial position, we can look forward to 2021 with great optimism.”

Operational Highlights for Q4 2020

  • New global agreement worth up to £370 million plus royalties with GlaxoSmithKline – to discover and develop selective, oral, small molecule agonists of GPR35 in inflammatory bowel disease and other gastrointestinal immune disorders.
  • Creation of new company – Tempero Bio – with specialist venture capital firm Aditum Bio (founded by ex-Novartis executives Joe Jimenez and Mark Fishman) – Tempero in-licensed Sosei Heptares’ Phase 1 mGlu5 negative allosteric modulator program to develop novel therapeutics targeting addiction and anxiety. Sosei Heptares received an upfront payment and strategic equity stake in Tempero Bio and is eligible to receive future development and commercial milestone payments plus tiered royalties from any future product sales.
  • New global agreement worth up to US$380 million plus royalties with Biohaven Pharmaceuticals – to develop, manufacture and commercialize novel, small-molecule CGRP receptor antagonists (including HTL0022562) for treating CGRP-mediated disorders.
  • New strategic technology collaboration with Captor Therapeutics focused on targeted GPCR degradation as a novel approach to drug design – initial program to identify small molecules degraders of a GPCR strongly implicated in gastrointestinal disorders.
  • Potent anti-viral compounds identified from the collaborative COVID-19 R&D program that was initiated during 2020 – several novel compounds, potentially broad-spectrum antivirals for COVID, identified are being optimized for preclinical studies having demonstrated high potency in inhibiting the activity of the SARS-CoV-2 Mpro protease as well as promising oral bioavailability.

Operational Highlights for the Full Year 2020

  • Approximately US$
    200
     million raised from an International Offering of shares and convertible bonds to pursue strategic growth initiatives including:
    • a potentially transformative acquisition to secure long-term revenue growth,
    • investments in novel technologies that complement and future-proof its drug discovery platform,
    • expansion of its drug candidate discovery and early development into new target classes, and
    • in-licensing late-stage clinical assets to develop for the Japanese market.

The balance of funds will support organic growth initiatives, and corporate purposes.

  • New global agreement signed with AbbVie, initially worth up to US$409 million plus royalties – initially a single-target discovery and option-to-license collaboration to discover novel small molecules targeting inflammatory and autoimmune diseases. AbbVie has the option to expand the collaboration up to a total of four targets.
  • Second novel drug candidate resulting from multi-target drug discovery collaboration with Pfizer entered clinical trials – first subject dosed with PF-07054894, a CCR6 antagonist targeting Inflammatory Bowel Disease, triggered US$5 million payment to Sosei Heptares.
  • Enerzair® Breezhaler® approved in Europe and Japan to treat asthma – Enerzair® is once-daily, first-in-class inhaled LABA/LAMA/ICS combination developed by Novartis, and in which Sosei Heptares has an economic interest. The achievement of these milestones triggered the payment of US$6.25 million to Sosei Heptares from Novartis.
  • Excellent scientific progress made with orexin agonist program in conjunction with spin-off companies Orexia and Inexia – progress building unique orexin modulator drug discovery and design engine triggered next tranche of funding from Medixci. Further orexin receptor structural data and insights generated to help optimize drug discovery targeting neurological diseases.
  • Measures put in place to successfully operate in response to the COVID-19 pandemic – policies and practises were rapidly implemented to ensure safety of employees and other stakeholders and to reduce the spread of coronavirus, while also prioritizing revenue-generating work for our major collaboration partners.

Post-period Highlights

  • Worldwide rights to out-licensed muscarinic agonist programs regained from AbbVie/Allergan – independent review of programs has completed, with increased investment allocated to advance the HTL0016878 selective muscarinic M4 agonist through clinical studies and build value ahead of future partnering. HTL0016878 represents a unique opportunity to develop a novel therapeutic with a new mechanism of action for neurological disorders including schizophrenia. Negotiations for collaborations on this and other muscarinic programs are now in progress.
  • New strategic technology collaboration with PharmEnable for AI-driven drug discovery – aim to identify new leads against a challenging “peptidergic” GPCR target
  • First strategic collaboration to explore SBDD approaches beyond GPCRs with Metrion Biosciences collaboration targeting ion channels, a large, under-exploited target class where structural input to drug discovery has been limited. Drug discovery program to identify novel, highly specific leads for further development against a single ion channel associated with neurological diseases.

Financial Highlights for the 12-month Period ended 31 December 2020

  • Revenue totalled JPY 8,842 million (US$82.8 million*), a decrease of JPY 884 million (US$6.4 million) vs. the prior corresponding period. Milestone revenues and upfront fees can vary considerably year on year and depend on the achievement of defined milestone events and the commencement of new partnership agreements within that year. Whilst four new out-licensing agreements were signed in 2020 vs. three in 2019, milestone receipts in 2019 from existing collaborations were larger, resulting in an overall drop in revenue. 2019 revenue included several major milestones, including a US$15 million milestone receipt from AstraZeneca.
  • Cash R&D expenses totalled JPY 3,411 million (US$31.9 million), a decrease of JPY 526 million (US$4.2 million) vs. the prior corresponding period. This was primarily related to a reduction in project activity due to COVID-19, as well as the successful recovery of excess costs incorrectly charged by one supplier. In the period under review, 96% of R&D spend related to our UK operations.
  • Cash G&A expenses totalled JPY 1,995 million (US$18.7 million), a decrease of JPY 169 million (US$1.2 million) vs. the prior corresponding period, and was primarily related to a reduction in our UK National Insurance liability linked to share based payments as a result of the reduction in our share price over the period.
  • Cash earnings** totalled JPY 2,904 million (US$27.2 million), an increase of JPY 58 million (US$1.1 million) vs. the prior corresponding period.  Whilst there has been a slight reduction in revenue year on year, the strong management of costs has been greater, leading to an increase in cash earnings.
  • Operating Profit totalled JPY 928 million (US$8.7 million), an increase of JPY 544 million (US$5.1 million) vs. the prior corresponding period.
  • Net profit totalled JPY 1,479 million (US$13.8 million), an increase of JPY 47 million (US$0.7 million) vs. the prior corresponding period. The main reason for the increase was due to the increase in  operating profit and net finance income.
  • Cash and cash equivalents increased by JPY 24,633 million from the beginning of the year and amounted to JPY 40,008 million as at December 31, 2020.
  • Net cash provided by financing activities for the period under review totalled JPY 20,278 million. This was primarily due to net cash inflows from the issuance of new shares raising JPY 5,145 million (including shares issued through an international offering) and the issuance of convertible bonds raising JPY 15,902 million.

*Convenience conversion to US$ at the following rates: 2020: 1US$ =106.774 JPY; 2019: 1US$ =109.035 JPY

**Non-IFRS measure

About Sosei Heptares

We are an international biopharmaceutical group focused on the discovery and early development of new medicines originating from our proprietary GPCR-targeted StaR® technology and structure-based drug design platform capabilities. We are advancing a broad and deep pipeline of novel medicines across multiple therapeutic areas, including neurology, immunology, gastroenterology and inflammatory diseases.

We have established partnerships with some of the world’s leading pharmaceutical companies, including AbbVie, AstraZeneca, Biohaven, Genentech (Roche), GSK, Novartis, Pfizer and Takeda and additionally with multiple emerging technology companies. Sosei Heptares is headquartered in Tokyo, Japan with corporate and R&D facilities in Cambridge, UK.

“Sosei Heptares” is the corporate brand and trademark of Sosei Group Corporation, which is listed on the Tokyo Stock Exchange (ticker: 4565). Sosei, Heptares, the logo and StaR® are trademarks of Sosei Group companies.

For more information, please visit https://soseiheptares.com/ 
LinkedIn: @soseiheptaresco | Twitter: @soseiheptaresco | YouTube: @soseiheptaresco

Enquiries:

Sosei Heptares
 – Media and Investor Relation
Hironoshin Nomura
SVP Investor Relations and Corporate Strategy
+81 (0)3 6679 2178
[email protected]

Shinichiro Nishishita
VP Investor Relations
Head of Regulatory Disclosures
+81 (0)3 5210 3399 
[email protected]

Citigate Dewe Rogerson (for Sosei Heptares)

Yas Fukuda – Japanese Media
+81 (0)3 4360 9234
[email protected]

Mark Swallow

David Dible – International Media
+44 (0)20 7638 9571 
[email protected]

Forward-looking statements

This press release contains forward-looking statements, including statements about the discovery, development and commercialization of products. Various risks may cause Sosei Group Corporation’s actual results to differ materially from those expressed or implied by the forward-looking statements, including: adverse results in clinical development programs; failure to obtain patent protection for inventions; commercial limitations imposed by patents owned or controlled by third parties; dependence upon strategic alliance partners to develop and commercialize products and services; difficulties or delays in obtaining regulatory approvals to market products and services resulting from development efforts; the requirement for substantial funding to conduct research and development and to expand commercialization activities; and product initiatives by competitors. As a result of these factors, prospective investors are cautioned not to rely on any forward-looking statements. We disclaim any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

 

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SOURCE Sosei Heptares

Xeris Pharmaceuticals Receives European Commission Approval of Ogluo™ (glucagon) Injection for the Treatment of Severe Hypoglycaemia in Adults, Adolescents, and Children Aged 2 Years and Over With Diabetes Mellitus

Xeris Pharmaceuticals Receives European Commission Approval of Ogluo™ (glucagon) Injection for the Treatment of Severe Hypoglycaemia in Adults, Adolescents, and Children Aged 2 Years and Over With Diabetes Mellitus

OGLUO™ Europe’s first and only ready-to-use liquid glucagon for rescue

First availability expected in the fourth quarter

Approval supported by data from pivotal Phase 3 study

CHICAGO & DUBLIN–(BUSINESS WIRE)–
Xeris Pharmaceuticals, Inc. (Nasdaq: XERS), a specialty pharmaceutical company leveraging its novel formulation technology platforms to develop and commercialize ready-to-use injectable and infusible drug formulations, today announced that the European Commission (EC) has approved Ogluo™ (glucagon) injection for the treatment of severe hypoglycaemia in adults, adolescents, and children aged 2 years and over with diabetes mellitus. The marketing authorisation is valid in all 27 countries of the European Union, plus Iceland, Norway, and Liechtenstein. As the EC decision was received after the end of the Brexit transition period, Xeris will complete a further administrative step in order to obtain a license in Great Britain. No re-examination of clinical data by the U.K. Medicines and Healthcare Products Regulatory Agency (MHRA) is expected.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20210212005054/en/

(Photo: Business Wire)

(Photo: Business Wire)

“This EU approval for Ogluo is a major milestone for Xeris and a significant advancement in the treatment of severe hypoglycaemia for the diabetes community in Europe. Hypoglycaemia is the #1 side effect of insulin, and severe hypoglycaemia is the most urgent emergency any person with diabetes could face. Ogluo, the first pre-mixed auto-injector for severe hypoglycaemia, can help offset the inherent risk associated with insulin,” said Paul R. Edick, Chairman and Chief Executive Officer of Xeris Pharmaceuticals. “We are preparing to launch Ogluo later this year, while simultaneously seeking a commercialization partner in which to broaden the availability of Ogluo to more European countries.”

The EC approval was supported by data from a Phase 3, multi-centre, randomized controlled, non-inferiority study. The study was conducted among 132 adults with type 1 diabetes in Europe and North America to evaluate the liquid stable glucagon auto-injector as a treatment for severe hypoglycaemic events compared with Novo Nordisk’s GlucaGen® HypoKit®. The results demonstrated comparable efficacy between the two groups in achieving a plasma glucose of greater than 3.89 mmol/L (>70 mg/dL) or a relative increase of 1.11 mmol/L (≥20 mg/dL) in plasma glucose concentration within 30 minutes of administration. The study also found that time to resolution of hypoglycaemia symptoms as well as time to resolution of the overall feeling of hypoglycaemia were comparable. No safety or tolerability concerns were noted. In this study, the most common adverse reactions were nausea and vomiting.

“Hypoglycaemia is a neglected complication of glucose-lowering therapy in patients with diabetes mellitus. Attempts made at intensive glycaemic control invariably increases the risk of hypoglycaemia. In patients experiencing severe hypoglycaemia an increase in deaths up to six-fold has been associated to diabetes in comparison to those not experiencing severe hypoglycaemia. Patients with diabetes should be evaluated for the risk of clinically important hypoglycaemia and have access to ready-to-use glucagon,” said Thomas Pieber, MD, Professor of Medicine, Chair, Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University of Graz, Austria.

ABOUT GVOKE/OGLUO

Gvoke® PFS and Gvoke HypoPen® (glucagon injection), the first prescription, ready-to-use, pre-mixed, pre-measured glucagon injection, were approved by the FDA in September 2019 for use in the United States. Gvoke is indicated for the treatment of severe hypoglycemia in pediatric and adult patients with diabetes ages 2 years and above. Ogluo received a positive opinion from the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) in December 2020 and the European Commission (EC) granted the marketing authorisation on 11 February 2021. Ogluo is indicated for the treatment of severe hypoglycaemia in adults, adolescents, and children aged 2 years and over with diabetes mellitus.

INDICATION AND IMPORTANT SAFETY INFORMATION FOR GVOKE

Gvoke is indicated for the treatment of severe hypoglycaemia in adult and paediatric patients with diabetes ages 2 years and above.

IMPORTANT SAFETY INFORMATION

Contraindications

Gvoke is contraindicated in patients with pheochromocytoma, insulinoma, and known hypersensitivity to glucagon or to any of the excipients in Gvoke. Allergic reactions have been reported with glucagon and include anaphylactic shock with breathing difficulties and hypotension.

Warnings and Precautions

Gvoke is contraindicated in patients with pheochromocytoma because glucagon may stimulate the release of catecholamines from the tumor. If the patient develops a dramatic increase in blood pressure and a previously undiagnosed pheochromocytoma is suspected, 5 to 10 mg of phentolamine mesylate, administered intravenously, has been shown to be effective in lowering blood pressure.

In patients with insulinoma, administration of glucagon may produce an initial increase in blood glucose; however, Gvoke administration may directly or indirectly (through an initial rise in blood glucose) stimulate exaggerated insulin release from an insulinoma and cause hypoglycemia. Gvoke is contraindicated in patients with insulinoma. If a patient develops symptoms of hypoglycemia after a dose of Gvoke, give glucose orally or intravenously.

Allergic reactions have been reported with glucagon. These include generalized rash, and in some cases, anaphylactic shock with breathing difficulties and hypotension. Gvoke is contraindicated in patients with a prior hypersensitivity reaction.

Gvoke is effective in treating hypoglycemia only if sufficient hepatic glycogen is present. Patients in states of starvation, with adrenal insufficiency or chronic hypoglycemia, may not have adequate levels of hepatic glycogen for Gvoke administration to be effective. Patients with these conditions should be treated with glucose.

Necrolytic migratory erythema (NME), a skin rash commonly associated with glucagonomas has been reported post-marketing following continuous glucagon infusion and resolved with discontinuation of the glucagon. Should NME occur, consider whether the benefits of continuous glucagon infusion outweigh the risks. Glucagon administered to patients with glucagonoma may cause secondary hypoglycemia.

Adverse Reactions

Most common (≥5%) adverse reactions associated with Gvoke are nausea, vomiting, injection site edema (raised 1 mm or greater), and hypoglycemia.

Drug Interactions

Patients taking beta-blockers may have a transient increase in pulse and blood pressure when given OGLUO. In patients taking indomethacin, Gvoke may lose its ability to raise blood glucose or may even produce hypoglycemia. Gvoke may increase the anticoagulant effect of warfarin.

Please see full Prescribing Information for Gvoke on www.xerispharma.com. Manufactured for Xeris Pharmaceuticals, Inc. by Pyramid Laboratories Inc., Costa Mesa, CA 92626.

About Glucagon

Glucagon is a metabolic hormone secreted by the pancreas that raises blood glucose levels by causing the liver to rapidly convert glycogen (the stored form of glucose) into glucose, which is then released into the bloodstream. Glucagon and insulin are two critical hormones in a glycemic control system that keep blood glucose at the right level in healthy individuals. In people with diabetes who are dependent on insulin, this control system is disrupted, and insulin must be injected to avoid high levels of blood glucose (hyperglycemia). The opposite effect, or low blood glucose (hypoglycemia), is also prevalent in this population due to dysregulated glucagon secretion. Severe hypoglycemia is a serious condition and can lead to seizures, coma, potential brain injury and, if untreated, death.

Glucagon is the standard of care for treating severe hypoglycemia. According to the American Diabetes Association, glucagon should be prescribed for all individuals at increased risk of clinically significant hypoglycemia, defined as blood glucose <54 mg/dL (3.0 mmol/L). Leveraging XeriSol™, one of Xeris’ two proprietary formulation technology platforms, Xeris has the potential to provide the first ready-to-use, room-temperature stable liquid glucagon for use by people with diabetes and other conditions to prevent or manage various forms of hypoglycemia and improve glucose control.

About Severe Hypoglycemia

Hypoglycemic events of any severity are a daily concern for people with diabetes. Mild or moderate hypoglycemia can occur multiple times a month. Severe hypoglycemia is characterized by severe cognitive impairment, requiring external assistance for recovery, and can be extremely frightening for patients and caregivers. Severe hypoglycemia can result in cardiovascular disease, seizure, coma, and, if left untreated, death. These severe hypoglycemic events can occur multiple times a year. Such events require emergency assistance from another person or caregiver such as a family member, friend, or co-worker.

About Xeris Pharmaceuticals, Inc.

Xeris (Nasdaq: XERS) is a specialty pharmaceutical company delivering innovative solutions to simplify the experience of administering important therapies that people rely on every day around the world. With a novel technology platform that enables ready-to-use, room-temperature stable formulations of injectable and infusible therapies, the company is advancing a portfolio of solutions in various therapeutic categories, including its first U.S. commercial product, Gvoke®. Its proprietary XeriSol™ and XeriJect™ formulation technologies have the potential to offer distinct advantages over conventional product formulations, including eliminating the need for reconstitution, enabling long-term, room-temperature stability, significantly reducing injection volume, and eliminating the requirement for intravenous (IV) infusion. With Xeris’ technology, new product formulations are designed to be easier to use by patients, caregivers, and health practitioners and help reduce costs for payers and the healthcare system.

Xeris is headquartered in Chicago, IL. For more information, visit www.xerispharma.com, or follow us on Twitter, LinkedIn or Instagram.

Forward-Looking Statements

Any statements in this press release about future expectations, plans and prospects for Xeris Pharmaceuticals, Inc., including statements regarding the market and therapeutic potential of its products and product candidates, expectations regarding clinical data or results from planned clinical trials, the timing or likelihood of regulatory approval and commercialization of its product candidates, the timing or likelihood of expansion into additional markets, the timing or likelihood of identifying potential development and commercialization partnerships, the potential utility of its formulation platforms and other statements containing the words “will,” “would,” “continue,” and similar expressions, constitute forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including, without limitation, the impact of COVID-19 on its business operations, its reliance on third-party suppliers for Gvoke® and Ogluo™, the regulatory approval of its product candidates, its ability to market and sell its products, if approved, and other factors discussed in the “Risk Factors” section of the most recently filed Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission, as well as discussions of potential risks, uncertainties, and other important factors in Xeris’ subsequent filings with the Securities and Exchange Commission. Any forward-looking statements contained in this press release speak only as of the date hereof, and Xeris expressly disclaims any obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise.

The Company intends to use the investor relations portion of its website as a means of disclosing material non-public information and for complying with disclosure obligations under Regulation FD.

Xeris Investor Contact

Allison Wey

Senior Vice President, Investor Relations and Corporate Communications

[email protected]

312-736-1237

KEYWORDS: Illinois Europe Ireland United States North America

INDUSTRY KEYWORDS: Biotechnology Pharmaceutical Managed Care Medical Supplies Health Diabetes Medical Devices Clinical Trials

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Mineral Resources and Mineral Reserves 2020

PR Newswire

BOLIDEN, Sweden, Feb. 12, 2021 /PRNewswire/ —

The Mineral Resources and Mineral Reserves situation in Aitik, Garpenberg and Kevitsa is stable. During the year, exploration continued to be successful at the Tara Deep mineralization and Mineral Resources in the Boliden Area increased as a result of exploration at the Rävliden deposit.

– “We have a stable situation in our major mines, and developments are advancing in Tara and the Boliden Area. Naturally, the fact that we’ve begun underground drilling in Tara is very good news,” says Stefan Romedahl, President, Business Area Mines.

The cost of exploration in 2020 was SEK 504 m (570). Some exploration activities were affected by restrictions related to Covid-19.

Aitik

No large-scale exploration is currently in progress in Aitik, however, mining preparation work is continuing with the Liikavaara deposit, around 3 km northwest of Aitik. Exploration and evaluation is also in progress at the Nautanen deposit, around 15 km north of Aitik. Mineral Reserves in Aitik, including Liikavaara, increased by 165 Mtonnes (14%) while Mineral Resources fell by 210 Mtonnes (19%). Design changes and a refined cost model have allowed the Mineral Resource to be converted to a Mineral Reserve. 42 Mtonnes were milled during 2020. New estimations of resources in Nautanen during 2020 showed an increase of 5.7 Mtonnes (36%).

The Boliden Area

In the Boliden Area, exploration at the Rävliden mineralization in Kristineberg continued. Drilling, test mining and metallurgical testing were carried out during 2020 and a new Mineral Resource estimation has shown an increase in the Mineral Resource by 2.7 Mtonnes. The Mineral Reserve increased in Renström but fell in Kristineberg and Kankberg. In all, the Mineral Reserves fell by 1.2 Mtonnes (9%), which is less than milled during the year (1.6 Mtonnes). The Mineral Resource increased by 2.7 Mtonnes (12%).

Garpenberg

Garpenberg has good advance planning with Mineral Resources and Reserves. Exploration and studies were successful during the year and the Mineral Reserve increased by 14.7 Mtonnes (20%). In Garpenberg, 3.0 Mtonnes were milled during 2020. Exploration in Garpenberg has contributed as much as was mined in 2020, but by promoting such large tonnages to Mineral Reserves, Mineral Resources have been reduced by 6.4 Mtonnes (9%).

Kevitsa

In Kevitsa, the Mineral Reserve decreased by 12 Mtonnes (9%), 9.5 Mtonnes of which was mined during the year. Design changes, including wider ramps and higher cut-offs for the next two years, have caused the remainder of the reduction. Conversely, the Mineral Resource increased by 22 Mtonnes (14%). New borehole information and a new geological model are the most important factors behind this increase.

Tara

Exploration at the Tara Deep mineralization continued with drilling from the surface, while drifting is underway toward Tara Deep at a depth of around 1000 meters. Drifting has progressed far enough that drilling toward Tara Deep has begun from underground. Drilling from the surface has been successful and Tara Deep is now estimated to include 26 Mtonnes of inferred Mineral Resources, compared with 22 Mtonnes in 2019, which has also contributed to an increase in Tara’s total Mineral Resource of 4.7 Mtonnes (16%). Meanwhile, work on improving the geological models of the mineralization and designing stopes in the Tara mine continues. Together with the contribution from drilling, this has resulted in the replacement of the entire year’s mining output of 2.3 Mtonnes and an increase in the Mineral Reserve of 700 Ktonnes (4%).

Calculation of Mineral Resources and Mineral Reserves, 2020

Boliden follows the recommendations of the Swedish Mining Association (SveMin) for reporting exploration results, Mineral Reserves and Mineral Resources and strives to report according to the Pan-European Reserves and Resources Reporting Committee (PERC). The PERC standard has clearer requirements for documentation and the competent persons who must evaluate the information that companies report. The transition to the PERC standard is a process that takes place during a transitional period until the company has had time to switch to using the PERC standard. As far as possible, this review is carried out in compliance with the PERC standard, but the reporting does not claim to be completely in accordance with the regulatory framework. All summarizing reports for Mineral Resources and Mineral Reserves per project and mine are reviewed and approved by competent persons presented in the relevant report. This summary of Mineral Resources and Mineral Reserves has been reviewed and approved by Gunnar Agmalm, Competent Person and Head of Ore Reserves and Project Evaluation, Boliden, which is a member of The Australasian Institute of Mining and Metallurgy (AusIMM) and The Fennoscandian Association for Metals and Minerals Professionals (FAMMP), both of which are approved organizations for competent persons according to PERC.

 


Planning prices                                  

                                   


Long-term prices 2020  

                                   


Change compared to 2019                                           

                                   

Zinc  

                                   

USD 2,400/metric ton  

                                   

Copper  

                                   

USD 6,600/metric ton  

                                   

Nickel  

                                   

USD 16,000/metric ton  

                                   

Lead  

                                   

USD 2,100/metric ton  

                                   

Gold  

                                   

USD 1,300/tr. oz  

 

 

+100

                                   

Silver  

                                   

USD 17/tr. oz  

                                   

Palladium  

                                   

USD 1,200/tr. oz  

 

 

+200

                                   

Platinum  

                                   

USD 1,000/tr. oz  

                                   

Cobalt  

                                   

USD 20/lb  

                                   

Tellurium  

                                   

USD 30/kg  

                                   

Molybdenum  

                                   

USD 8/lb  

                                   

USD/SEK  

 

8.0

                                   

EUR/SEK  

 

9.35

                                   

EUR/USD  

 

1.17

   

This information is information that Boliden AB is obliged to make public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of Director Communications, at 07.49 CET on February 12, 2020.

For further information, please contact:
Klas Nilsson, Director Group Communications, phone: +46 70-453 65 88

Boliden is a metals company with a focus on sustainable development. Our roots are Nordic, our market global. Our core competence lies within the fields of exploration, mining, smelting and metal recycling. Boliden has more than 5,700 employees and an annual turnover of SEK 50 billion. The share is listed in the Large Cap segment on NASDAQ OMX Stockholm 



www.boliden.com

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Press release (PDF)

 

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Biotage AB (publ) Year-End report January – December 2020

Double-digit organic growth

PR Newswire

UPPSALA, Sweden, Feb. 12, 2021 /PRNewswire/ — October – December

  • Net sales amounted to 298.1 MSEK (288.6), an increase by 3.3 percent, and organically* an increase by 10.0 percent.
  • Operating profit amounted to 59.6 MSEK (37.9).
  • The operating margin amounted to 20.0 percent (13.1).
  • Result after tax amounted to 44.4 MSEK (18.5).
  • Earnings per share was 0.68 SEK (0.28) before and after dilution.
  • The cash flow from operating activities increased to 87.5 MSEK (76.3).
  • Net cash* at December 31 was 157.0 MSEK (net debt -69.2).
  • Cash and cash equivalents amounted to 371.3 MSEK (185.9).
  • Liabilities to credit institutions amounted to 110.0 MSEK (109.6).
  • On November 4 the Board of Directors announced that a decision was taken to not convene an Extraordinary General Meeting to decide on dividends due to the continued uncertainty concerning the effects of the Corona pandemic.

January – December

  • Net sales amounted to 1,092.3 MSEK (1,101.4), a decrease by 0.8 percent, and organically* an increase by 1.4 percent.
  • Operating profit amounted 206.2 MSEK (208.1).
  • The operating margin amounted to 18.9 percent (18.9).
  • Result after tax amounted to 175.31) MSEK (186.8).
  • Earnings per share was 2.691)SEK (2.87) before and after dilution.
  • The cash flow from operating activities amounted to 279.0 MSEK (211.8).
  • On August 18 the Board of Directors decided to carry out a new share issue and to repurchase 243,313 class C shares in accordance with the resolution of the Annual General Meeting.
  • On August 31 it was announced that the total number of shares increased by 243,313, corresponding to 24,331.3 votes after the new issue of class C shares, and that the shares had been repurchased.
  • The Board of Directors intends to propose to the Annual General Meeting a dividend to the shareholders for 2020 of 1.50 SEK (0) per share, corresponding to 55.8 percent of the result after tax. According to the dividend policy Biotage shall distribute at least 50 percent of the net profit.

Comments by the CEO 

Double-digit organic growth -a record quarter

It is with immense pride that I present this report on the last quarter and the full year 2020, especially under the challenging conditions caused by the ongoing Corona pandemic (COVID-19).

I note with satisfaction that we after the second and third quarters, that were greatly affected by the pandemic, now once again deliver a strong quarter. In fact, our sales are the highest ever in a single quarter, for the full year this means continued organic growth for the Group. For the fourth quarter the reported sales were 3.3 percent higher compared to the corresponding period 2019, which organically was a 10.0 percent increase. For the full year the corresponding figures were a decrease by 0.8 percent and an organic growth by 1.4 percent.

The operating margin, EBIT, improved by 6.9 percentage points in the quarter compared to last year and achieved a margin of 20.0 percent.

For the full year the EBIT margin amounted to 18.9 percent, the same as last year.

It was our largest single product area, Organic chemistry, that contributed the most to the success in the fourth quarter, as its share of our sales increased by no less than 7 percentage points, from 46 to 53 percent, and 51 percent for the full year. All geographical areas except Japan showed growth for these products in the fourth quarter. The Asian countries had the strongest development, but it is also worth noting that the US came back strongly with a double-digit percentage sales increase and a record for the quarter.

Biotage’s Scale-up product area saw a sales decrease, which was due to a reduction of CBD sales in the US. Instead, we focused resources and activities on parties active in vaccine manufacturing. This contributed to increased sales and some recovery for Scale-up, which we see as very positive. We have long striven to broaden our customer and application base for the area and we have now further strengthened this work.

Many of our customers in the Analytical chemistry product area are among those who have been hit hard by the consequences of the pandemic. This applies in particular to commercial laboratories working with the analysis of patient samples. Here, however, we saw a gradual increase in activity levels during the quarter, which hopefully may indicate a trend break.

Another effect of the covid-19 pandemic was that Biotage’s sales and beta testing in the Biomolecules product area was limited as we had fewer opportunities to visit customers. A commercial launch of our automated plasmid purification system at maxi, mega and giga scale is approaching and is planned for the first half of 2021.

Our product mix continued to have an overweight of system sales in the quarter, accounting for 51 percent. Great sales successes for our purification systems in all regions except Japan contributed to this.

Geographically we continue to build a stronger presence in Asia. China and South Korea remain double-digit growth markets for Biotage. We also see great potential in India which, however, was hard struck by the restrictions resulting from the pandemic. Fortunately, we still noted a strong recovery of the operations in India in the latter part of the year. In Japan sales did not meet our expectations, but also here we saw positive signs with increased sales in the last quarter. After two quarters with weaker figures, the Americas ended the year with recovery in the last quarter, and I am very delighted to see that EMEA showed growth both in the quarter and the full year.

Looking at important investments during the year, we have expanded the machinery with automation solutions at our production unit in Cardiff, UK to strengthen manufacturing capacity. This work will continue in 2021. Furthermore, we have started work on the completion of a completely new building in Cardiff. It will be used primarily for the production of various types of consumables, with improved and more efficient production flows. We expect the first part of the expansion to be completed in the summer of 2021.

We are investing in efficiencies also in our production of the PhyTip® consumables in the Biomolecules product area in the US. In 2020 we started a project to introduce automation solutions that are currently undergoing production tests. We expect to be able to deploy them in the spring of 2021.

For our future development it is reassuring to see our strong balance sheet with a net cash of 157.0 MSEK, which is a 226.2 MSEK improvement compared to last year’s net debt of 69.2 MSEK. Through focused work we have improved our operating capital by 9.2 MSEK compared to the last full year.

The year has certainly been very challenging for us all, professionally as well as on the private level. For many the Covid-19 pandemic has blurred the boundary between home and workplace. This has been and continues to be a challenge in terms of work environment issues and the balance between work and leisure. Throughout this period, Biotage has constantly been working to maintain a high level of information to the Group’s employees, both on the global level and as country specific instructions in the various regions. We have utilized digital meetings and tried to facilitate homework for all employees by providing mobile computers, screens, office chairs, etc.

It is our assessment that we will continue to live with the limitations of the pandemic also in 2021. Through the lessons we take with us from this time, we are likely to work differently also when the pandemic is finally over. During the pandemic we have learned to work with greater flexibility. We have also travelled less both within and across national borders, which contributes to diminishing our environmental footprint and to increasing sustainability. We have developed new methods of working and been forced to be innovative and swift in order to overcome various problems.

Finally, I would like to take this opportunity to thank all our talented employees who, despite very challenging external circumstances, have enabled the Group to continue to perform at such a high level. Biotage is well positioned and I am very much looking forward to continuing with another successful year 2021.

Uppsala February 12 2021 

Tomas Blomquist

President and CEO

Calendar

Interim report January – March 2021

April 28 2021

Annual General Meeting 2021

April 28 2021

The Annual Report for 2020 is planned to be published

Week 14 2021

Interim Report January – June 2021

July 16 2021

Interim report January – September 2021

October 28 2021

Year-end report 2021

February 11 2022

All financial reports are published at www.biotage.com

The interim report for Biotage AB (publ) has been issued by the Company’s President and CEO Tomas Blomquist after authorization by the Board of Directors.

Uppsala February 12, 2021
Tomas Blomquist
President and CEO

For further information:

Tomas Blomquist, President and CEO
phone: +46 705 23 01 63                                                                                                                    

Annette Colin, CFO
phone: +46 703 19 06 76       

This information is information that Biotage AB (publ) is obliged to make public pursuant to the EU Market Abuse Regulation and the Securities Markets Act. The information was submitted for publication, through the agency of the contact persons set out above, on February 12, 2021 at 08:00 CET.

Biotage in brief

Biotage is a Global Impact Tech Company committed to solving society’s problems. We offer workflow solutions and products to customers in drug discovery and development, analytical testing and water and environmental testing.

Biotage is contributing to sustainable science with the goal to make the world healthier, greener and cleaner – HumanKind Unlimited.

Our customers span a broad range of market segments including pharmaceutical, biotech, contract research and contract manufacturers as well as clinical, forensic and academic laboratories in addition to organizations focused on food safety, clean water and environmental sustainability.

Biotage is headquartered in Uppsala in Sweden and employs approx. 485 people worldwide. The Group had sales of 1.092 MSEK in 2020 and our products are sold in more than 70 countries. Biotage’s share (BIOT) is listed in the Mid Cap segment on the NASDAQ Stockholm.

Website: www.biotage.com

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New 10K/15K Resolution Line Scan Image Sensors from ams Enable Higher Throughput in Optical Inspection Systems

New 10K/15K Resolution Line Scan Image Sensors from ams Enable Higher Throughput in Optical Inspection Systems

News facts:

  • 4LS line scan image sensors operate at speeds up to 120,000 lines per second
  • Independent lines of RGB + Clear sensor channels support full-color reproduction; digital TDI capability for excellent image quality in dim light
  • 4LS supports rigorous quality and process controls in next-generation smart factories

PREMSTAETTEN, Austria–(BUSINESS WIRE)–
ams (SIX: AMS), a leading worldwide supplier of high-performance sensor solutions, today launches the 4LS series, adding new faster and higher resolution line scan image sensors to its broad family of sensors for machine-vision applications. Use of cameras equipped with 4LS sensors will help operators of the latest smart factories to maintain the highest standards of quality control while increasing the volume of production output.

Offered in versions with 10K and 15K resolutions, the 4LS image sensors feature four Red/Green/Blue/Clear channels scanning at up to 120,000 lines per second. The 4LS series offers the system designer flexibility to meet various application requirements. Each of the four lines may be independently controlled and operated simultaneously for full-color image capture. Camera manufacturers can also implement 4:1 digital TDI (Time Delay and Integration) to achieve high image quality in low lighting conditions, or to perform high-speed object inspection. In addition, the sensors offer the choice of either an 8-bit or 12-bit LVDS output to provide the most appropriate trade-off between image quality and speed. Full well-charge options range from 10 ke- to 40 ke- to enable use in a wide range of illumination conditions.

The introduction of new faster, higher-resolution line scan image sensors creates a new opportunity for industrial-camera manufacturers and machine-vision system developers to add value to their products by enabling higher throughput and more effective optical inspection in applications such as: print inspection; continuous-surface and web inspection; food sorting and quality control; display inspection; and glass inspection.

Peter Vandersteegen, Segment Marketing Manager at ams, said: “ams has built a strong market position and an enviable reputation in the field of line scan image cameras with ams Dragster sensors. Now the launch of the 4LS image sensors provides designers of line scan image cameras a new option to increase scanning speeds and to support improved full-color image reproduction.”

ams delivering 1D/2D/3D technologies for machine vision

Machine vision encompasses a wide range of applications in factory automation, Automatic Identification and Data Capture (AIDC), volume and distance measurement, motion analysis, intelligent transportation systems, and document scanning. In addition to the Dragster and new 4LS line scanning sensor products, ams offers several product families addressing an ongoing need for various machine-vision applications and use cases in 1D/2D/3D. A more recent application is the vision of the environment for ever more complex autonomous robots and cobots.

“ams is a leader for VCSEL-based illuminators and high quantum efficiency NIR image sensors,” says Pierre Laboisse, Executive Vice President Global Sales and Marketing, ams. “This equipment benefits from accurate 2D, and ideally 3D visualizations of the environment and object to be worked with. Near infrared illumination, both with flood- and high-contrast dot illuminators, combined with sensitive NIR image sensors enables compact, cost effective, and high-performance 3D systems immune to uncontrolled illumination conditions.”

Compatible interface for family of camera products

The 4LS line scan image sensor is supplied as a Chip-on-Board (CoB) module mounted on a mechanically robust and thermally stable Invar package. The PCB interfaces of the 4LS 10K and 4LS 15K are fully compatible and interchangeable, allowing line scan camera manufacturers to build a family of products with different resolutions.

Pixel size in the new 4LS line scan image sensors is 5.6µm x 5.6µm. Dynamic range is up to 54dB, and quantum efficiency is 61% at 530nm.

ams continues to supply the Dragster series of line scan image sensors, which are available in single-line and two-line versions, and with resolution ranging from 2K to 16K.

The four-line 4LS line scan sensors are in volume production and are available for ordering via ams authorized distribution partners. For more technical information or for sample requests, go to https://ams.com/4LS.

Amy Flécher

Vice President Marketing Communications / ams AG

[email protected]

ams.com

KEYWORDS: Austria Europe

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Boliden’s fourth quarter: Strong earnings and cash flow for the quarter

PR Newswire

BOLIDEN, Sweden, Feb. 12, 2021 /PRNewswire/ — Revenues for the fourth quarter amounted to SEK 16,170 m (12,972) and operating profit, excluding revaluation of process inventory, totaled SEK 3,043 m (1,721). Free cash flow totaled SEK 2,750 m (822). For the full year, revenues amounted to SEK 56,321 m (49,936) and operating profit, excluding revaluation of process inventory, totaled SEK 8,438 m (7,035).

“A very good quarter. At our mines, development in Kevitsa is particularly positive, while production at the smelters has been characterized by a high level of stability,” says Mikael Staffas, President and CEO.

The operating profit in Business Area Mines increased to SEK 1,858 m (890), mainly due to higher grades and overall good production. The milled volume in Kevitsa increased by more than 30% compared to the fourth quarter of 2019 and in Garpenberg 3.0 Mtonnes were milled in 2020, which is in line with the current environmental permit. Aitik’s milled volume was in line with the previous year, but has not yet reached the new design capacity. The Boliden Area’s earnings were positively affected by a good ore mix with a high proportion of gold, while production in Tara was affected by maintenance and some disruptions. The Kylylahti mine was closed down during the quarter, and the mine is now being prepared for reclamation and the concentrator is being mothballed.

Within Business Area Smelters, operating profit, excluding revaluation of process inventory, increased to SEK 1,109 m (759) as a result of higher volumes. In Rönnskär, production of most metals increased compared to the corresponding period last year due to good process stability and new capacity. In Harjavalta, copper production was also higher than in the fourth quarter of 2019 after completed investments, while production of nickel in matte was slightly lower. Zinc production in both Kokkola and Odda was characterized by high stability and was higher than in the previous year. Production in Bergsöe was lower than the corresponding period last year due to poorer supply and lower quality of input materials.

At the start of 2021, Boliden submitted an application for membership in the International Council on Metals and Mining (ICMM). The aim of membership is to work with other member companies to develop the industry’s work on various aspects of sustainability.

For further information, please contact:

Klas Nilsson, Director Group Communications, tel.: +46 70 453 65 88

Boliden is a metals company with a focus on sustainable development. Our roots are Nordic, our market global. Our core competence lies within the fields of exploration, mining, smelting and metal recycling. Boliden has around 6,000 employees and an annual turnover of SEK 50 billion. The share is listed in the Large Cap segment on NASDAQ OMX Stockholm.

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Boliden: Q4 Interim Report and Year-end report for 2020

PR Newswire

BOLIDEN, Sweden, Feb. 12, 2021 /PRNewswire/ —

 Q4 2020

  • Revenues totaled SEK 16,170 m (12,972) 
  • The operating profit totaled SEK 3,077 m (1,744)
  • The operating profit, excluding the revaluation of process inventory, totaled SEK 3,043 m (1,721)
  • Free cash flow totaled SEK 2,750 m (822)
  • Earnings per share totaled SEK 8.60 (4.97)

Strong earnings and cash flow during the quarter 

  • Stable production in Mines and Smelters.
  • The Board of Directors proposes a payment to the shareholders of SEK 14.25 per share through:
    • oan ordinary dividend of SEK 8.25 (7.00) per share.
    • oan extra payment of SEK  6.00 (0.00) per share through automatic share redemption.

Please find enclosed the full report.

The Interim Report will be presented via a webcast/conference call on Friday, 12 February at 09:30 (CET). Information is available at www.boliden.com.


Contact persons for information:

Mikael Staffas, President & CEO  

Tel: +46 8 610 15 00

Håkan Gabrielsson, CFO   

Tel: +46 8 610 15 00

Olof Grenmark, Director Investor Relations

Tel: +46 70 291 57 80

This information is information that Boliden AB is obliged to make public pursuant to the EU Market Abuse Regulation. The information was submitted for publication, through the agency of Director Investor Relations, at 07.45 CET on 12 February, 2021.

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