Our experts will update you every month with the latest updates and trends in clinical studies. Thus, you will always have essential information on the design and conduct of clinical trials, as well as practical tips for successful collaboration at the interfaces to other areas.
This online training programme consisting of three recorded webcasts will train you how to develop documents, compile them and submit an eCTD step by step.
These recorded six webcasts enable you to deal with the legal challenges in marketing authorisation and life cycle management.
Do you need to be well versed in European pharmacovigilance for your daily work? Then we recommend this e-Learning. You can choose between three different packages according to your level of expertise and requirements.
This e-Learning programme will focus on stability testing for chemical and biological products in the ICH region.
This e-Learning programme will familiarise you with the data requirements in CTD Module 3.