Bioanalytical Methods and Good Laboratory Practices (GLP) - Essential Elements for Pre-Clinical Studies during development of Drugs 2017 is a seminar that covers topics such as:
- Myths and Regulatory Expectations about GLP
- 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
Bioanalytical Methods and Good Laboratory Practices (GLP) - Essential Elements for Pre-Clinical Studies during development of Drugs 2017 brings together:
- 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