Catch up with the TOPRA Annual Symposium session on the Globalisation of Pharmaceutical Regulation over a lunch hour or any time that suits your schedule.
This is the first in a series of Online catch-up courses from TOPRA’s major meetings, designed for members who were unable to attend in person – or who did attend and want to revisit the session later.
Find out from the regulators themselves about the procedures used by the US FDA, the European Medicines Agency (EMA) and the Japanese Pharmaceuticals and Medical Devices Agency (PMDA) for sharing information and areas of collaboration.
From the Berlin 2015 TOPRA Annual Symposium session there are two video presentations Globalisation of Pharmaceutical Regulation:
- An update on the Japanese PMDA Office of International Programs
- How the EMA shares information between health authorities
Frequently asked questions
What do I have to do to complete the course?
To complete the course you view two videos, after this you will have the opportunity to contribute two discussion points and view other people's responses and ideas. Once you have completed the course you will receive a completion certificate.
How many CPD hours will I receive?
We recommend that this course should take you 2 hours to complete, you will therefore receive 2 CPD hours upon completion.
To register, please log in or create an account
Please read the training terms and conditions before booking onto this course. By booking a place on this course you are agreeing to the training terms and conditions.
Course price (including VAT):
Non member: £70+VAT
All fees are shown in Pounds Sterling and do not include VAT