Conference Date: 11 Oct 2010
Conference Ref: TD N10-8110
Fee: £450 + VAT
Venue: MWB Cavendish Square, London, W1
Designed with SME customers in mind, our new training days deliver the high quality training that you have come to expect from Management Forum, at a more accessible price.
When you download the brochure details of this course together with others in the same series will be provided.
Course Summary
The important role of Technical Documentation is increasing and this course is designed to enable delegates to learn more about the new initiatives in the format and review of Technical Documentation for Medical Devices. It is relevant to all who have to compile and review such documentation.
Gain essential practical advice through workshops and discussion on the new initiatives applicable to Technical Documentation.
Key Topics to Include:
- Contents of Technical Files and Design Dossiers
- STED format
- Technical File and Design Dossier Review
- Competent Authority Expectations
- Notified Body Role and Expectations
- Changes Resulting from Directive 2007/47/EC
Who Should Attend:
- Regulatory Affairs Personnel
- Quality Assurance Professionals
- Design Personnel who input into Technical Documentation
- Technical File Reviewers
Tutor:
Will Burton, Director, RSQA
Please contact andrea.james@management-forum.co.uk if you wish to know more about the new Training Academy or click here to visit our Training Academy Blog.
Click here to register for this important seminar.