Good Laboratory Practices (GLP) regulations and their distinction from the current Good Manufacturing Practices (cGMP) regulations
Challenges with complying with GLP regulations
Achieving Compliance with GLP regulations
Validation of Bioanalytical Methods
Bioanalytical methods and their distinction from Biological methods
Validation of Biological, Immunochemical and other Methods used to evaluation clinical samples
Who should Attend
Contract Testing Laboratories performing toxicology and pharmacology studies
Managers and Scientists involved in Drug Development from Pharmaceutical and Biotech Industry
Personnel from Laboratories testing Clinical samples for determining efficacy of drugs and biologics
Personnel from Laboratories performing Bioanalytical methods
Past Events
Bioanalytical Methods and Good Laboratory Practices (GLP) - Essential Elements for Pre-Clinical Studies during development of Drugs 2017 - 15-16 Jun 2017, San Francisco, California, United States (67414)
Important
Please, check "Bioanalytical Methods and Good Laboratory Practices (GLP) - Essential Elements for Pre-Clinical Studies during development of Drugs" official website for possible changes, before making any traveling arrangements
