PEGS

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.

PEGS

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.

PEGS

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.

Cosmetics GMP

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.

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.

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.

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.

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.

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.

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.