Programme
Regulatory Requirements of analytical procedure & validation
Dr Norbert Handler, RD &C Research, Development & Consulting
How to overcome some of the challenges when analysing Biological Drug Substances and Products
Thomas Fechner, Agilent
Analytical Quality by Design Through the Lifecycle
Patrick Jackson, GSK
State-of-the-Art evaluation of potency bioassays
Klemens Weitenthaler, VelaLabs - A Tentamus Company
Process for automatization of a Bioassay
Dr Marcus Gutmann, Microcoat Biotechnologie
Application of fast and non-destructive analysis techniques in quality and in-process control
Prof. Dr. Hartwig Schulz, formerly Julius Kühn-Institut (JKI)
Lectin Array – a novel technology for investigation of pharmaceutical products
Markus Roucka, VelaLabs - A Tentamus Company
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E-Mail: info@gmp-compliance.org
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