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PUBLICATIONS

European Biopharmaceutical Review

 

European Biopharmaceutical Review (EBR) is a journal designed to fill a unique position in scientific publishing. Published quarterly, it provides a dedicated platform of communication and information for the European biopharmaceutical market across Europe, North America & the rest of the world.

With editorial consisting of in-depth articles, case studies, meeting and report reviews written by specialists with hands-on experience in the biopharmaceutical industry, traditional multi-national pharmaceutical companies, investment houses and industry-associated governmental, economic and societal bodies. Each quarterly edition examines topical areas of importance across the board of biopharmaceutical research and development, with regular feature sections on BioBusiness Development, Research and Innovation, BioDiscovery, BioManufacturing plus special focuses on geographic or therapeutic territories.

For further information please contact:

Editorial

Jasmin Collier


 

 

 
  

Connect with us on Twitter: follow @EBRmagazine

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Featured in this issue
BioDiscovery
Biomarkers and Diagnostics

The Secrets in our Cells


Diamond Light Source’s Mary Cruse
sheds light upon recent work undertaken in cancer research, and the prospect of tailoring treatment to the genetic codes of any given patient – stating that perhaps the successful cure lies in each individual’s chemistry.
CELL-BASED RESEARCH
Cell Disruption

Under Pressure


Technology that performs mechanical lysis and homogenisation of cells are often sold on the basis of the pressure they are able to reach. Recent research undertaken by Dr Matthew Lougher of Constant Systems, however, demonstrates that the success of mechanical cell disruptions depends on much more than pressure.
  INDUSTRY DYNAMICS
Comment: Shipment Conditions

How Strong is a Peptide Bond?


Have you ever wondered how much you could save on your logistics costs? According to Dr Henk J Bak at Eurosequence, there is a simple solution: bidding farewell to outdated methods and adopting more relevant shipping procedures.

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Edited by
Dr Deborah O'Neil,
Chief Executive and Scientific Officer,
NovaBiotics Ltd
Published quarterly in
January, April,
July and October


 

Industry Events

2016 PDA Universe of Pre-filled Syringes and Injection Devices

17-18 October 2016, Hyatt Regency Huntington Beach Resort and Spa | Huntington Beach, CA

At the 2016 PDA Universe of Pre-filled Syringes and Injection Devices, industry and regulatory experts will share their experiences, new developments, regulatory considerations, challenges, and industry trends and best practices. This is a must-attend event for all industry professionals involved in the development, manufacturing, testing or marketing of pre-filled syringes and injection devices.
More info >>

 
News and Press Releases

ClinDatrix Contract Research Organisation Launches Oracle Health Sciences InForm 6.1 and Oracle Argus 8.0 to Speed Clinical Trials and Support Global Safety Collection and Risk Management Efforts


More info >>

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White Papers

Sourcing Commercial Drugs for Clinical Trials: US vs. EU Understanding the Differences

Myoderm

Sourcing commercial drugs for clinical trials is a dynamic process. There are many factors to consider: single source or regional sourcing, strategy, price, supply availability, lead times, and documentation are just a few. In the past, there were fewer clinical trials that required commercial drug sourcing, so demand was not as high. Today, the demand for commercial drugs in clinical trials has greatly increased and, as a result, inventory is tighter, orders are monitored more closely by manufacturers, and lead times have increased. This report highlights the key differences in sourcing from the US and EU.
More info >>

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