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.

Main activities

• 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.