Veterinary Pharmacovigilance

Understand the relationship between pharmacovigilance and the processes of application and registration

  • TBD

2 days course

English

11.200,- DKK ex VAT
(app. 1.506,- EUR ex VAT)

At the moment there is no available dates for this course.

Module 8

Summary

This course will help you understand the basic principles of pharmacovigilance and provide you with a comprehensive overview of the basic elements in pharmacovigilance in relation to veterinary medical products.

After the course, you will be able to analyze and evaluate methods and data in adverse event reporting. You will also be able to evaluate regulations and guidelines in veterinary pharmacovigilance.

You will know how to use best practices in veterinary pharmacovigilance working processes, prepare adverse event reports, design appropriate pharmacovigilance working methods, and operate in a dynamic and changing environment.

The course is offered every 3 years. 

Keywords

The legislative framework for veterinary pharmacovigilance
The pharmacovigilance (PV) management systems
Adverse events reporting
VeDDRA terms
Causality assessment
Electronic reporting
Post-marketing safety surveillance
The Periodic Safety Update Report (PSUR)
Audits and inspections
Signal detection
Risk management

What you will learn

  1. The basic principles of pharmacovigilance and the basic elements of pharmacovigilance in relation to veterinary medical products
  2. How to analyze and evaluate methods and data in adverse event reporting and how to evaluate regulations and guidelines in veterinary pharmacovigilance
  3. How to use best practices in veterinary pharmacovigilance working processes, prepare adverse event reports and design appropriate pharmacovigilance working methods in a dynamic and changing environment

What your company will get

  1. A safety and pharmacovigilance professional who understands the basic principles of pharmacovigilance and can provide a comprehensive overview of the basic elements of pharmacovigilance in relation to veterinary medical products
  2. A safety and pharmacovigilance professional that can independently analyze and evaluate methods and data in adverse event reporting
  3. A safety and pharmacovigilance professional that can independently analyze and evaluate regulations and guidelines in veterinary pharmacovigilance and play an important role in any interdisciplinary project team
  4. An employee who can provide valuable input on veterinary pharmacovigilance

Registration quick facts

You can pay by credit card or by invoice. We charge the amount shortly after you register. If you cancel your registration more than 30 days prior to the course, you will receive a full refund. Read our cancellation policy.

Yes, if you experience any technical problems, please call us at + 45 39 27 60 60, or send us an email at contact@atriumcph.com

If you cancel your registration more than 30 days prior to the course, you will receive a full refund. If you get sick on the day of the course, you can hand over your seat to a colleague. To hand over your seat, please contact us at +45 39 27 60 60. Read our cancellation policy.

Want to know more about this course?

Contact Programme Director Gitte Hornemann Møller at +45 39 15 09 20

Send an email

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