Open training courses for medical device manufacturers
We provide training courses specifically for medical device manufacturers and their suppliers. Our current courses are listed below. Please click on the course of interest for more information including dates available. Courses can booked and paid for on line by clicking on the date for the course required, or by calling +44 (0)115 921 6200 or by using the downloadable booking form on this page. If you have a discount code (except early bird), bookings can only be made over the telephone. We accept all major credit and debit cards (except American Express).
Our Training Courses
- CE Marking - An Introduction to the Medical Devices Directive
- Compilation of a Technical File / Design Dossier
- Risk Management 1 - ISO 14971
- Risk Management 2 - Usability Engineering and Electrical Medical Equipment
- Biological Evaluation of Medical Devices ISO 10993-1
- ISO 13485 Internal Auditor
- Sterilization - Steam (Advanced)
- Sterilization - Ethylene Oxide (Advanced)
- Sterilisation - Gamma & Electron Beam (Advanced)
- Designing for Sterilization
- Cleanroom Good Manufacturing Practices (GMP)
- FDA Pre Market Notification - 510(k) registration
- FDA Quality System Inspection Technique (QSIT)
New courses in 2012 - Cleanroom GMP (25th Jan 12 & 19th July 12); Quality System Inspection Technique (QSIT) (26th June 12 & 6th December 12); FDA Pre Market Notification - 510(k) Registration Process (21/22 February 12 & 10/11 October 12); Sterilization - Steam Advanced (27 March 12 & 23 October 12); Risk Management -BS EN 62366 Usability Engineering & BS EN 60601-1 Electrical Medical Equipment (25 April & 22 November 12 )
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Download 2011/12 training course brochure Download the booking form
More courses are available inhouse
