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By: Medicom Consulting  05/12/2011
Keywords: training courses, Medical Device, Public Training Courses

Book now to secure your place on our remaining public training courses in 2011 Dates to be announced soon

Process Validation
Device Design
QS Regulation

Book now to secure your place on our remaining public training courses in 2011 at iSmithers, UK.

Medical Device Legislation and Material Selection

Book now to secure your place on our remaining public training courses in 2011 at DS Certificering, Copenhagen, Denmark.

Process Validation

Medical Device Design and Development Control

Establishing Compliance With ISO 11135-1:2007 for Validation of Ethylene Oxide Sterilization

Keywords: Device Design, Medical Device, Public Training Courses, training courses

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05/12/2011

Quality System Regulation 21 CFR Part 820

Each delegate is provided with a course manual containing comprehensive notes on topics presented, and copies of relevant regulations and guidance documents are provided for the use of delegates during the course. The FDA Quality System Regulation 21 CFR Part 820 was published on Monday October 7th, 1996, and came into effect on June 1st, 1997, while the Design Control requirements came into full effect on June 1st, 1998.