The pharmaceutical industry is highly regulated. Mastering and controlling all steps in pharma regulatory and registration procedures are pivotal to successful market entry. Medial’s knowledge of local industry requirements and established relationships with Government Regulatory Agencies ensure that all steps in the registration procedure are handled professionally and as swiftly as possible. We ensure the continuous follow-up of all registration activities at all times. Our services include Pharma dossier validation, verifying and assuring the match between the dossier and specific information required by some countries, consultation in listing (orphan drugs, reimbursement etc.) and other regulatory questions, submission and follow-up of pharma dossiers until the respective governmental authorities grant registration.