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PharmTech Europe
11 February 2020

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TOP STORIES

The Call for a Rapid Response

Bio/pharma researchers mobilize to diagnose and treat patients in pandemic threat.
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Catalent to Acquire MaSTherCell Global for $315 Million

Catalent builds on its investment in cell and gene therapy development and manufacturing with the acquisition of MaSTherCell Global.
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Industry News

Stevanato Group to Partner with Pfeiffer Vacuum Technologies

The companies plan to provide characterization testing of container-closure systems for the biopharma industry.
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Guidance on Biosimilar Licensure

FDA published draft guidance for applicants seeking licensure of a proposed biosimilar or proposed interchangeable biosimilar.
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Regulatory News

Coronavirus Offers Opportunities and Challenges for Biopharma R&D

The research community is moving quickly to launch clinical trials of potential countermeasures, while regulatory authorities aim to support product development through regulatory flexibility.
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FDA Approves Seqirus’ Adjuvanted, Cell-Based Pandemic Influenza Vaccine

The vaccine is designed to provide active immunity against the influenza A (H5N1) strain and can be easily deployed in a pandemic event.
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Bio/Pharma News

Aimmune to License Monoclonal Antibody for Food Allergy Treatment

Aimmune plans to introduce the antibody as an adjunctive treatment with its Characterized Oral Desensitized ImmunoTherapy programmes to research treatment outcomes in patients with food allergies.
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Otsuka, PhoreMost Team Up for Drug Discovery

Otsuka will use PhoreMost’s phenotypic screening platform to identify new targets for drug development, with a focus on gene therapy.
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Supplier News

Hitachi Chemical Opens New Cell and Gene Therapy Manufacturing Facility

The new facility includes six classified environment rooms with space to expand.
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Horizon Discovery Licenses Knockout CHO Cell Line to NGM Biopharmaceuticals

The knockout CHO K1 cell line will be used to support biotherapeutic R&D across a range of therapeutic indications.
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FEATURED TOPICS

VIEWPOINTS

Of Serious Concern?

Amid the rapidly rising cases of a novel coronavirus, concerns are being raised over preparedness and potential disruptions to the pharma supply chain.
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FORMULATION

Improving Solubility of Cannabinoids

Lipid-based solutions offer a natural approach to improving the solubility of cannabinoid-derived products.
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EUROPEAN REGULATORY WATCH

Brexit: What Happens Next for Pharma?

The UK and Europe are entering a transitional period, which will involve negotiations across the board, including those on the pharma regulatory landscape.
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MANUFACTURING

Designing Commercial-Scale Oligonucleotide Synthesis

Consider current large-scale practices for oligonucleotide synthesis as a basis for improving commercial-scale platform strategies.
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PRODUCT PROFILE

Stoelzle Glass Group

Safe Packaging for Healthy Products
Pharma bottles are an integrated part of the final medicine. That’s why Stoelzle cares that much about quality and reliability when manufacturing safe packaging for healthy products in soda lime Type III quality.
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TAKE THE SURVEY

17th Annual BioPlan Associates' Biopharmaceutical Manufacturing Report

Expert input is needed for the bio-industry's most in-depth, global benchmarking and analysis study, which examines current global and regional trends affecting the bioindustry. Participants who complete the survey receive a free aggregated summary of the study results, a free whitepaper on the Top 15 Trends in Biopharmaceutical Manufacturing, and the opportunity to share insight about trends in biomanufacturing. For each completed survey, BioPlan Associates will contribute $10 (up to $3000) to a global health charity.
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Events

Bioprocessing Summit Europe

Barcelona, Spain

24–26 March 2020

SMI Group's 3rd Annual Injectable Drug Delivery Conference

London, UK

13–14 May 2020

more events

eBOOKS

Regulatory Sourcebook and Reference, September 2019

Pharmaceutical Technology’s Regulatory Sourcebook and Reference highlights regulatory trends and enforcement actions, risk-based studies for analytical procedure validation, and generic drug applications, as well as a detailed analysis of pharmacopoeia requirements, challenges with compliance.

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