REGULATORY AFFAIR
We provides professional, technical and administrative services to helping the companies in laboratory, clinical studies and regulatory affairs. We are able to support our clients, both for entire or individual stages of their projects, in preparing studies protocols, conducting and monitoring specific studies, to support data analysis and assist with document compilation and reports writing. We guarantee continuous update on EU and national legislation.
Farefarma S.r.l. proposes you the following services:

• Expertise on safety and efficacy of veterinary medicines for drug registration (Part IIIA and Part IIIB)
• Bibliographic evaluation and food-residues risks assessment for active ingredients with no MRL
• User safety and user risks assessment