Services What we Offer Regulatory Approvals FDA 510(K) CDSCO Medical Devices Registration in India CDSCO Import License CDSCO Manufacturing License CE Marking SFDA UK CA BIS Certification Design & Development Documentation Drug Device Combination Products US FDA 21 CFR 820.30 Design Control Requirements Turnkey Project Consultants Product Feasibility & Detail Project report Manufacturing Facility Validation Documentation Clean Room Guidance Quality Managment System FDA 21 CFR Part 820 Quality System Regulation ISO 13485 - QMS Medical Device ISO 15378 Certification | Primary Packaging Regulatory Consulting MDSAP CONTACT US TODAY BOOK YOUR APPOINTMENT START YOUR PROJECT
