This one day seminar is aimed at QA staff in drug products manufacturers and especially their QPs who have specific responsibilities under directive 2004/27/EC. Participants will learn about the legislators’ perspectives and the key differences between APIs and products, which lead to different audit techniques and thought processes when auditing API manufacturers.

The seminar includes: the background to current GMPs for APIs , FDA and EU interpretation of GMPs for APIs , specific opportunities from the guidelines that API manufacturers may exploit , specifics of what to look for when auditing an API site.