Presented by
Management Forum

Periodic Safety Update Reports for Veterinary Medicinal Products

Including requirements for regions including the EEA, USA, Canada and Australia and an update on the implications of Brexit *NEW EVENT!*

Find out more

  • Format: Bespoke training
  • CPD: 12 hours for your records (depending on your requirements)
  • Certificate of completion

Course overview

Periodic safety update reports (PSURs) are pharmacovigilance documents intended to provide a comprehensive and critical evaluation of the riskbenefit balance of a veterinary medicinal product at defined time points after its authorisation, taking into account new or emerging safety information in the context of cumulative information on risk and benefits. Regulatory authorities assess information in PSURs to determine if there are new risks identified for a veterinary medicine and/or if its risk-benefit balance has changed. A PSUR assessment can determine if further investigations on a specific issue are needed, or if an action is necessary to protect animal health (eg an update of the information provided to animal healthcare professionals).

This interactive two-day seminar will provide a comprehensive, yet practical, assessment of the main requirements for PSURs in the European Economic Area (EEA), USA and other geographic regions. Content and format of the PSUR will be covered in depth, and key legislation and guidelines will be reviewed in order to ensure a compliant reporting company. The programme will also include workshops on PSURs for the EEA, USA and Australia. This is an excellent opportunity to gain essential information for your company to ensure compliance with the PSUR requirements.

Benefits of attending:
  • Understand the requirements of periodic safety update reports (PSURs)
  • Know the format and content of PSURs
  • Establish who is responsible
  • Plan your management and assessment of PSURs
  • Be updated on the implications of Brexit
  • Understand the requirements of periodic drug experience reports (PDERs) in the USA
  • Compare the differences between PSURs and PDERs
  • Discover the requirements of other countries
  • Consolidate learning with practical workshop sessions

Who should attend?

The event will be beneficial to all those with some experience of veterinary pharmacovigilance who require essential training on PSURs including:

  • Adverse event monitoring officers
  • Drug safety officers
  • QPPVs and deputy QPPVs
  • Personnel from regulatory affairs and registration departments

The course can be used as part of the training to become a QPPV or Deputy QPPV.

Declan O'Rourke

Declan O’Rourke has over 20 years’ experience in industry where he has held technical, marketing, product development, clinical development, production and pharmacovigilance roles.

He is a veterinary surgeon, holds a Diploma in Marketing, a Master of Business Administration and a Fellowship of the Royal College of Veterinary Surgeons. He now directs Ortec PV Consultancy Ireland specialising in pharmacovigilance and represented IFAH-EU in the VICH Working Group on pharmacovigilance.

He is Honorary Associate Professor in Veterinary Pharmaceutical Development at Nottingham Veterinary School and Past President of British Cattle Veterinary Association.

More details

We don't have any currently scheduled dates for this course but we can customise it to your requirements and deliver it on an in-house basis for any number of your staff or colleagues.

See below or contact us to discuss yor requirements.

Multiple colleagues?
Talk to one of our training experts to discuss how to:

Run this course conveniently and cost-effectively in-house for your staff and colleagues

Aleksandra BEER
Training expert

+44 (0)20 7749 4749