When: 22 February 2022
Time: 9.00-12.30 GMT
Overview
The Veterinary Medicines Regulation will see a new pharmacovigilance system set into place which will require a number of changes to requires a number of changes to the signal management area, PSURs and how we handle the non-serious adverse events during the transition period. This workshop will cover the legislative requirements and practicalities, as well as offering an opportunity for discussion with both industry professionals and regulators.
Learning objectives
During this workshop, we will cover:
- Overview of the Pharmacovigilance system
- How will transition to the new system happen
- Changes to signal management
- Introduction to the Masterfile approach
Target Audience
Professionals working in European veterinary medicines regulatory affairs or placing products on the European market:
- At all levels of experience
- Involved with originator or generic products
CPD
This course offers 2.5 CPD hours for successful completion. To learn why CPD is important visit our Lifelong Learning page.
How do I register?
Prices
Type |
Member |
Non-member |
Standard |
£70 + VAT |
£95 + VAT |
Discounted Places
A limited number of discounted places are available at the rates below for those:
Please email meetings@topra.org for a discount code before making your booking.
Type |
Member |
Non-member |
Discount |
£35 + VAT* |
£47.50 + VAT* |
* VAT, if applicable, is charged at a rate of 20%.
Terms and conditions
By purchasing this webinar, you are agreeing to the terms and conditions.