Services What We Offer 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 Regulatory Approvals FDA 510(k) Indian Import License CE Making SFDA Registration Design & Development Documentation Drug Device Combination Products US FDA 21 CFR 820.30 Design Control Requirements CONTACT US TODAY BOOK YOUR APPOINTMENT START YOUR PROJECT
