• Overall Project Planning (veterinary or human drugs), in accordance with current regulations
• Regulatory strategy in product development
• Product Overview: Study of the market and possible patents
• Dealing with the Regulatory Agencies: Representation and dialogue with the regulatory authorities
• Submission of Registration dossiers (electronically): Application for marketing authorization from the regulatory authorities
• Updating the Registration Dossier: Variations of the conditions of authorization, Approvals, Renewals, Pharmacovigilance (postmarketing studies)
• Drafting of the Drug Master File of active ingredients: preparation and presentation thereof
• Expert Reports and tabular formats
• Training
• Scientific and technical audit:

 - Of the Registration dossier: compliance at all times with current legislation
 - Expert Reports and tabular formats

LOUFARM manages any transaction with the Regulatory Agencies (national, European or extra-community)