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PharmTech Europe
16 June 2020

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TOP STORIES

COVID-19 Update

Updates on COVID-19 vaccine candidates, FDA policies, company partnerships, and more.
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Fujifilm Corporation to Invest $928 Million into Fujifilm Diosynth Biotechnologies’ Denmark Site

The investment will increase production lines for bulk drug substance and will add a fill/finish production line to the site.
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Industry News

EC Pledges Nearly $340 Million Additional Vaccine Funding to Gavi

The European Commission is pledging EUR 300 million (US$339 million) to Gavi for vaccines for infectious diseases, in addition to an earlier pledge of more than EUR 1.5 billion (US$1.7 billion) made on May 4, 2020.
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Report Shows UK Public Support Relaxed Vaccine Regulations

According to a report from commercial law firm, Hill Dickinson, there is general support by the public of the United Kingdom that vaccine regulations should be relaxed in light of the current COVID-19 pandemic.
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Regulatory News

EMA Validates MAA for Leo Pharma’s Tralokinumab

Leo Pharma, medical dermatology specialist, has announced that the European Medicines Agency (EMA) has validated its marketing authorization application (MAA) for tralokinumab.
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EMA Gives Positive Opinion on J&J Investigational Preventive Ebola Vaccine Regimen

Johnson & Johnson’s Janssen Pharmaceutical Companies has received a positive opinion in Europe for its two-dose Ebola vaccine regimen.
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Bio/Pharma News

AstraZeneca, Accent Therapeutics in $1.1-Billion Deal for RNA-Modifying Protein Therapeutics

The collaboration will focus on novel therapeutics targeting RNA-modifying proteins for cancer treatment.
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Siemens and Exyte Collaborate to Provide Modular Biopharma Facilities

Siemens and Exyte partner for fast-track construction of modular, automated, digitalized biopharmaceutical facilities.
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Supplier News

Supplier Operations Status Report

Suppliers to the bio/pharma industry are sharing news about the business operations during the global COVID-19 pandemic. To view current information about the company’s business operations, click the company name.
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Oxford Biomedica Signs Agreement with Vaccines Manufacturing and Innovation Centre

Oxford Biomedica, has signed a collaboration agreement with the not-for-profit organization, the Vaccines Manufacturing and Innovation Centre, to provide the UK with its first strategic vaccine development and advanced manufacturing capability.
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FEATURED TOPICS

FORMULATION

Formulating for Convenience and Compliance

The correct mix of excipients is crucial to the success of fast dissolving/orally disintegrating dosage forms.
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ANALYTICS

The Importance of Partnering for Bioanalytical Studies

Bioanalytical studies are an important aspect of biologic drug development that may necessitate partnering with bioanalysis experts.
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MANUFACTURING

Why Do Disinfectant Residues Matter?

Consider how to assess the risks of disinfectant residues and understand their possible sources.
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DRUG DELIVERY

Better Connected: The Value of Connected Drug Delivery

Connected delivery solutions can provide value to the industry and patients, through improved medication adherence and outcome optimization.
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PRODUCT/SERVICES PROFILE

Process2Clean®: Process Cleaning Detergents

VAI’s Process2Clean®, Process Cleaning Detergents, are designed to remove process residues that could contaminate or adulterate further product manufacturing in the pharmaceutical, biotechnology, medical device, and research & development industries.
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WEBCAST

Dry Powder Inhalers: Key Considerations for Combination Product Development

Wednesday June 24, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST
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Events

Bioprocessing Summit Europe

Barcelona, Spain

21–23 July 2020

SMI Group's 3rd Annual Injectable Drug Delivery Conference

London, UK

2–3 September 2020

CPhI Worldwide

Milan, Italy

13–15 October 2020

more events

eBOOKS

Regulatory Sourcebook and Reference, December 2019

In Pharmaceutical Technology's ongoing Pharmacopoeia Compliance Series, experts explain the revision process for global and national pharmacopoeias, best practices for monitoring changes, and how to participate in revisions. Other features include FDA warning letters, building a quality culture, and essentials for DOE and QRM.

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