How to handle a regulatory inspection to avoid FDA-483 issues 2014
20 Aug 2014
Webinar
Description
Topics
Good record keeping for GMP and non-GMP studies
Determine the sequences of an inspection
Presenting clear and concise information
Establish a process of handling an inspection
Keep clear and concise records of observations
Train your personnel to handle an inspection
Determine your compliance weaknesses
Who should Attend
Regulators
Analytical chemists
Researchers who are involved in inspections
Past Events
How to handle a regulatory inspection to avoid FDA-483 issues 2014 - 20 Aug 2014, Webinar (46261)
Important
Please, check "How to handle a regulatory inspection to avoid FDA-483 issues" official website for possible changes, before making any traveling arrangements
