Date: On-demand - This is a recording of the live webinar which took place on 6 July 2016.

Learning outcomes

After attending this webinar, participants should be able to:

• Be familiar with the different types of variations and their requirements
• Prepare and submit veterinary variations via the different EU procedures in the European Economic Area (EEA)

Topics

• Variation types and categorisation 
• Grouping and worksharing of variations 
• Current EU legislation and guidelines for national, MRP, DCP and CP applications
• Practical experience on quality, safety, efficacy and pharmacovigilance variations
• Preparation and submission of variation in the EEU
• Update of dossier versions

Target audience

Personnel in the registration and regulatory affairs departments of the veterinary pharmaceutical industry dealing with regulatory submissions in the EEA.

Why attend?

This webinar will provide an overview of the veterinary EU variation legislation and available guidance; including advice on the preparation and submission of variations applications.

CPD

This course offers 1 CPD hour for successful completion, to learn about why CPD is important visit the Lifelong Learning page.

Speakers

• Dr Luisa Pachés Samblás, Regulatory Procedures Team Leader at Cyton Biosciences Ltd
• Pascale Canning, Regulatory and Communications Executive at Cyton Biosciences Ltd
• Joshua Forster, Regulatory Executive at Cyton Biosciences Ltd. 

Pricing

• Members: £75.00 + VAT
• Non-members: £95.00 + VAT 

Terms & conditions