During your traineeship, you will participate in the implementation of the Veterinary Medicines Regulation (EU) 2019/6 (VMP-Reg).
The Veterinary Medicines Regulation (EU) 2019/6 (VMP-Reg) introduces for the first time the legal basis for granting marketing authorisations for products intended for limited markets with specific provisions, in order to promote the availability of VMPs within the Union for minor species or for the treatment or prevention of diseases that occur infrequently or in limited geographical areas.
The implementation of the new legal provisions will involve:
• the review of the approach for eligibility for ‘limited market’ product (establish objective criteria) to ensure that it is aligned with the intentions of the Regulation;
• the review and update existing technical guidance on reduced data requirements (safety, efficacy of all VMPs except immunologicals);
• continue ongoing work on MUMS classification and applying reduced data requirements and financial incentives in accordance with the agreed policy.
To be eligible for consideration for this placement, you are required to:
For criteria 1 and 2, you will be required to provide proof in the application form and at the interview stage. Failing to present these documents may result in the disqualification from the procedure.
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