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The 2013 PEGS event offers six streams in the areas of protein & antibody engineering, oncology, expression, analytical, safety, and purification. These highly focused streams enable researchers to discuss and find solutions to challenges faced in the lab and hear research that has yet to be published. Conference short courses offer a primer or in-depth workshop on everything from phage and yeast display to immunogenicity and protein therapeutics. A biologics partnering forum will also be offered for both emerging companies with innovative technologies and established companies seeking collaborations.
New Webinar: Challenges in Implementing ICH Q6B for Biologics Characterization
This webcast will provide an overview of the requirements outlined in ICH Q6B, Specifications: Test Procedures and Acceptance Criteria for Biotechnological/Biological for analytical characterization of biological products.
1 More Events
Free conference about ISO 22716 certification and GMP audit of cosmetics.
3rd Annual Outsourcing Clinical Trials
At Arena International we go to extreme lengths to get to know our audience and cater to their specific needs and wishes. The OCT team lives and breathes conferences in the biotech and pharma space, allowing us to create truly innovative and inspired events.
SGS US Biopharm Seminar 2013
Biopharmaceuticals – From Characterization to Clinic, a half-day seminar to discuss advances in Biopharmaceutical development.
SSC MDD and PPE Seminar
Society for Clinical Trials (SCT) Annual Meeting
The Society for Clinical Trials, created in 1978, is an international professional organization dedicated to the development and dissemination of knowledge about the design, conduct and analysis of government and industry-sponsored clinical trials and related health care research methodologies.
AAPS National Biotech Conference
Please come visit us at booth #100.
Medical Devices Directives (93/42/EEC) and Technical File Preparation Workshop
Held with Singapore Manufacturing Federation, the 2 day workshop is to familiarize delegates with the requirements of Directive 93/42/EEC as amended by Directive 2007/47/EEC and to allow manufacturers of medical devices to ensure continued compliance.