Within the framework of the company’s development strategy and in line with veterinary pharmaceutical regulations, handle all technical-regulatory affairs, registrations and relations with the various administrative authorities regarding the MA and advertising.
- Define and implement the defence and extension programme for existing and upcoming registrations.
- Draw up the annual plan for submission of MA application files to the administrations.
- Ensure product files meet regulatory requirements.
- Provide monitoring and internal communication on changes in French and European regulations for all subjects relating to product registration.
- Consult authorities and experts.