ISO 13485 Quality Management for Medical Devices ISO 13485 is the internationally recognized standard designed to help manufacturers comply with regulatory systems and understand what they need to do to place compliant devices on markets throughout the world. Find out how to be certified to ISO 13485
Introduction to ISO 13485 Medical Devices £580 + VAT 1 days classroom based training Discover the importance of ISO 13485 on an international scale Understand how you can better meet customer and regulatory requirements View details for Introduction to ISO 13485 Medical Devices
ISO 14971 Medical Device Risk Management £650 + VAT 1 days classroom based training Identify links between ISO 13485 and ISO 14971 and learn how risk management applies to the product lifecycle Define risk management terminology and objectives View details for ISO 14971 Medical Device Risk Management
CE Marking of Medical Devices training £1805 + VAT 3 day classroom training course Understand the legal and operational aspects of European CE Marking in line with the European Medical Devices Directive (MDD) Increase EU market access and boost customer confidence View details for CE Marking of Medical Devices training
BS EN ISO 14155:2011 Clinical investigation of medical devices for human subjects. Good clinical practice Price: £196.00 Members price: £98.00 Buy a copy of BS EN ISO 14155:2011
BS EN 80001-1:2011 Application of risk management for IT-networks incorporating medical devices. Roles, responsibilities and activities Price: £184.00 Members price: £92.00 Buy a copy of BS EN 80001-1:2011
BS ISO 15223-2:2010 Medical devices. Symbols to be used with medical device labels, labelling, and information to be supplied. Symbol development, selection and validation Price: £140.00 Members price: £70.00 Buy a copy of BS ISO 15223-2:2010
