Dr. Raymond Munden has over 30 years experience in pharmaceutical research and development and was formerly Head, Analytical Services Europe for GlaxoSmithKline. He has led project teams that developed many new chemical entities and their pharmaceutical products that were successfully taken to market. Dr. Munden is an expert in stability protocol design and testing, stability storage facilities, experimental design and degradation chemistry. He is now a consultant for all aspects of pharmaceutical development.
Have fronted GLP and GMP inspections by regulatory inspectors and carried out numerous audits of pharmaceutical development laboratories and contract laboratories. Skilled presenter who has run many training courses internationally.
Specialties: Knowledgeable about all aspects of pharmaceutical development, especially Pharmaceutical Analysis and an acknowledged expert in validation and in stability testing.