MRP and DCP Procedures - Specific National Requirements
Specific national requirements
New applications in MRP/DCP
The electronic format (eCTD) is the format for the submission of all applications for marketing authorisation.
Full electronic dossier should be submitted via CESP to HALMED.
Detailed list of national requirements:
- Written statement by the future MAH (if not seated in Croatia) naming its local representative seated in Croatia with the contact details,
- Proof that the future MAH has responsible person for Pharmacovigilance seated in Croatia authorised by the Agency or proof that application for his/her approval has been submitted to the Agency (this submission should be separate from the submission for marketing authorisation),
- Proof that fee for the procedure has been paid.
