Support all regulatory aspects of assigned veterinary vaccine and biotherapeutic projects
Provide regulatory guidance and strategy in relation to new product development (including advice on study protocols and reports). Draft requests for scientific advice
Review and critique documentation intended for regulatory submissions to ensure relevant regulatory requirements are met
Compile and draft registration dossiers suitable for global markets, in collaboration with other subject matter experts where needed
Support submissions in target countries and lead regulatory activities to obtain and maintain licenses
Support all types of product lifecycle activities (draft and compile renewals, variations, post-authorisation commitments etc.)
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