BSI Medical Device Regulatory Update Seminar
08:30 AM - 16:30 PM
BSI is hosting their Medical Devices Regulatory Seminars mid to late November for medical device manufacturers, regulatory affairs and quality assurance staff. Their full-day Medical Device Seminars are focused on the European medical device regulatory and quality assurance landscape, sharing current experience, best practice and the latest expectations from the perspective of the Notified Body for CE Marking, ISO 13485 and MDSAP certification.
For more information and to register, click here.
Procurement, Regulatory and International issues are critical to our future success and the association brings enormous value in these key areas.Simon Talbot (Managing Director P3 Medical Ltd )