This semiars informs you what to focus on to be well prepared for your next GCP audit in Biostatstics.
This advanced seminar is designed as an advanced course and will focus on all relevant topics for an expert in the field of medical scientific information. Our speakers will update you on all the applicable key issues.
Our global and local experts will update you every two months with the latest regulatory and legislative developments. Thus, you will always have the essential information and trends in regulatory affairs and pharmacovigilance at your fingertips!
This course will show you how to write scientific documents, for instance a clinical evaluation or technical documentation respectively, in good English, readable style and target-oriented manner, meeting on the same time regulatory requirements.