Different requirements for Phase I Investigational Drug Products: 2018 is a seminar dedicated to which GMPs apply since most Phase I drugs are exempt from full GMP requirements and what IND data requirements are necessary as a result?.
Who should Attend
Regulatory Management or Regulatory Specialists
Quality Associates or Specialists
Quality Auditors
Compliance professionals
R & D Scientists- chemists, geneticists, biochemistry specialists, formulation chemistry
Validation Engineers
Senior Quality Managers, Quality VPs
Laboratory Personnel
Past Events
Different requirements for Phase I Investigational Drug Products: 2018 - 10-11 May 2018, Hilton Garden Inn Salt Lake City Airport, Utah, United States (73484)
Important
Please, check "Different requirements for Phase I Investigational Drug Products:" official website for possible changes, before making any traveling arrangements
Event Categories
Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Medical device, Medical laboratories, Medical technology, Pharma
