This course is for you, particularly if involved in: Regulatory affairs Project management Business planning Commercial Managers Manufacturing and QA Labelling and artwork Medical information Clinical Pharmacovigilance
Benefits of Attending
WHY YOU SHOULD ATTEND
This course will provide an up-to date overview of the European pharmaceutical regulatory environment, procedures and obligations. You will learn about the legal basis of regulation, development strategies and the strategic importance of pre-submission actions, the format for presentation of data, how the registration procedures work and post authorisation strategies and obligations.
It will be of value for regulatory affairs personnel and also for those who interact with regulatory personnel in order to understand action time-lines and information requirements
GBP EUR USD Standard 1399 1959 2182 Early 1199 1679 1870 Excluding VAT @ 20.00% Book by 6 Feb to get the early booking price shown above.