Veterinary medicines follow a strict regulatory framework to ensure the wellbeing of animals and to keep animals healthy in the food chain for human consumption.
This course is designed for the regulatory professional to give a complete guide to the regulatory guidelines surrounding the authorisation of veterinary medicinal products in the EU. The course will provide you with fundamental regulatory knowledge to help you unpick the complexity of the system and apply your knowledge to achieve fast product approval and effective product maintenance.
You will explore the regulatory landscape for veterinary medicines and examine the European licensing procedure for product approval. You will discuss in detail the submission process, analysing areas such as quality and efficacy.
Live Online Academies
Gain real-time access to a subject matter expert delivering online training in a structured virtual classroom environment. Live online academies are virtual versions of some of our most popular face-to-face courses, delivered in bitesize sessions of 1.5-3 hours online.
Over 4 sessions students will learn through:
- Live interactive bitesize sessions
- Direct interaction with the trainer during live sessions
- Participation in interactive features within sessions including polls, Q&A, break out rooms, tasks, case studies, and more
- Revisiting recorded sessions with unlimited access for 30 days
- Interaction with peers during live sessions and through the online forum
Timings and dates are subject to change - final confirmation will be provided with login details. Delegates will receive login instructions within a week of the course start date. If you have any questions please contact email@example.com.
What will you learn?
Understand and successfully apply the latest directive to your marketing authorisations
Choose the right submission procedure to support your application
Establish your veterinary pharmacovigilance reporting systems
Packaging & Labelling
Packaging & Labelling
Comply with the latest regulations for packaging and labelling of veterinary medicinal products
Learn how to maintain your marketing authorisation with a practical guide to variations
Who is this course for?
This course has been specifically designed for those working in the development of new veterinary medicinal products
- Regulatory Affairs
- Document Management
- Project Managers in Regulatory Affairs
- Research & Development
Engaging in Continuing Professional Development ensures that both academic and practical qualifications do not become out-dated or obsolete; allowing individuals to continually ‘up skill’ or ‘re-skill’ themselves, regardless of occupation, age or educational level. This course has been assessed and is CPD certified.