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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
iso 13485 | 21 cfr part 820 | Majakel Medical | Device Consultant
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Majakel Medical provides iso 13485, 21 cfr part 820 and complete medical device solution by practical and professional medical device consultant.
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