Services WHAT WE OFFER Turnkey Project Consultants Product Feasibility & Detail Project report Manufacturing Facility Validation Documentation Clean Room Design Quality Managment System FDA 21 CFR Part 820 Quality system Regulation ISO 13485 - QMS Medical Device ISO 15378 Certification | Primary Packaging Regulatory Consulting MDSAP Regulatory Approvals EDA Registration FDA 510(K) CDSCO Registration CE Marking SFDA UK CA 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
