iso 13485 | 21 cfr part 820 | Majakel Medical | Device Consultant

Project Planning Quality Engineer- ing Quality System Development Regulatory support for FDA Outsourcing: Manu- facturing, Docu- ments and People majukel+ Process Valida- MEDICAL +44 01633 680979 O +44 07528 578004 Risk Management for the system including Software Design and Devel- opment of Medical Devices CERTIFIED [email protected] Supplier Devel- opment 21 cfr part 820 Medical device iso 13485 consultancy