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European Medicines Agency to keep its current place in the European Commission

Under the responsibility of the directorate general for health

Europe | Regulatory

Employing new single-use technology in bioprocesses

There has been considerable progress in the application of single-use technologies in biopharmaceutical production. CMO Rentschler Biotechnologie discusses recent advances

Europe | Biotechnology | Manufacturing

Johnson & Johnson makes commitment to speed up Ebola vaccine development

Will invest US$200m to expand production at Janssen Pharmaceutical Companies

Europe | North America | R and D | Therapeutic Sector | Vaccines

Roche to invest CHF3bn over next 10 years at its Basel site

Will build modern research infrastructure, attractive offices and develop a sustainable site

Design and Build | Europe | Manufacturing

Lyophilisation: meeting new demand and challenges

Armin Dalluege, General Manager of Wasserburger Arzneimittelwerk, a subsidiary of Recipharm, in Wasserburg, Germany, highlights trends in drug lyophilisation

Manufacturing

The growth of mPEG technology

With an increase in the number of innovator companies looking to outsource the development and manufacture of mPEGs, Dr. Reddy’s (CPS) discusses what to look for in a potential outsourcing partner

Drug Delivery | R and D | Biotechnology | Manufacturing

Aston University to tackle multidrug resistance targets in collaboration with Calixar

They will study the extraction, stabilisation and crystallisation of full-length human ABC transporters

Europe | R and D | Therapeutic Sector

Cloud-based eTMFs – less paper, more value

With regulatory pressure mounting, pharma companies should need no help deciding to migrate to paperless trial master files. For those thinking about switching, Rik van Mol, Vice President of R&D Strategy, Veeva Systems, outlines the key considerations for making the transition

Information Technology

ATCC adds new customer-driven format to its quality control standards portfolio

Makes it easier for industrial and pharmaceutical labs to test for product safety

North America | Regulatory | Measurement and Analysis

Incorporating CMOs into the clinical trial supply chain

The clinical supply chain involves working with several outsourced partners. Jens Mattuschka, Vice President, CLS Worldwide Operations, Parexel International, looks at core planning to reduce the risk of failure

Regulatory | R and D | Manufacturing

In the Press