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Introduction

The course covers the requirements of the Medical Device Regulatory Standard ISO 13485 and the regulatory framework and documentation required to market a medical device. Those attending will get an understanding of the requirements and documentation required to market and maintain compliance for medical devices in the market place. There are tutorials on the Directives, the regulatory system, the marketing of a device and the ISO 13485 Medical Device Standard. Added to this there is an introduction to risk management and the vigilance system. The course is interactive with many practical exercises and discussions.

Venue

Reading Scientific Services Limited (RSSL)

Reading Scientific Services Limited (RSSL), The Science & Technology Centre, Whiteknights Road, Earley Gate, Reading, RG6 6BZ, United Kingdom

Organised by

Reading Scientific Services Limited

Contact information

Mrs Rachel Horton
The Science and Technology Centre, Earley Gate, Whiteknights Road, Reading, RG6 6BZ, United Kingdom
01189184076
Contact us by email

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