About
This webinar will explore current topics in the regulation of medicines advertising and is targeted at but not limited to; pharmaceutical companies and their agents involved in advertising development and sign-off. Those involved in advertising and marketing of medicines, medical affairs and regulatory affairs.
At this webinar participants will learn:
- How to make sure advertising is compliant
- Vetting procedures
- Common problems identified from casework
- The latest regulatory updates, particularly changes following the departure of the UK from the EU
CPD credits: 2 credits available for full attendance.
Questions For The Panel
Once you have registered, you will have the opportunity to submit pre-event questions to our panel of speakers via the Delegate Area. You will be issued with login details on your registration confirmation email. The team will endeavour to answer as many of these questions as they can at the event.
To submit your questions, please log into the Delegate Area and go to Panel Questions in the menu.
Delegates will also have the opportunity to also submit their questions at the live event.
Twitter - #HotTopicsinAdvertising22
- Tweets will appear here soon
Agenda
Please note agenda timings are subject to change.
Hot Topics Agenda — full schedule
March 17th, 10:30 - 12:30
Welcome and Introduction
Beryl Keeley — AIMS Group Manager, MHRA
Review of the year: What's new?
Beryl Keeley — AIMS Group Manager, MHRA
Getting it right: Top tips from vetting
Claire Tilstone — Advertising Standards & Outreach Unit Manager, MHRA
Learnings from 2020 vetting casework for prescription and OTC medicines
Self-Regulation 1: PMCPA
Heather Simmonds — Director, PMCPA
Report on PMCPA casework and the ABPI Code
Self-regulation 2: PAGB
Laura Kelly — Advertising Services Manager, PAGB
Review of PAGB initiatives, with a focus on digital content
Panel session
Panel: MHRA, PMCPA, PAGB
Webinar close
Speakers
Register
Please check back for registration information.