European countries comprising of 31 nations have their own national requirements, Fees requirements, Different language as well as various additional optionss, Making the regulatory filings very complex. Nuvo is designed to assist you sail through complex requirements with ease. Our team is ready to support you with following activities to write file and get approval of submission for marketing licenses maa 1. Guidance in best procedure to adopt for filing a maa2. Dossier writing for maa as per ich in ectd. 3. Submission maa to european countries consistent with the schedule mrp. Dcp, Via national and cp. 4. Interaction with regulatory medical institutions for procedural matters. 5. Booking slots for marketing authorization application for mrp and dcp. 6. Conversion of ctd or nees format to ectd.