M4 - Pre & Post Market Technical File Data - The Design History File for Medical Devices (QP)

About this course

One day course for quality and regulatory compliance professionals involved in the management of the design of medical devices. This course will enable the delegate to understand the requirements for Design History (particularly from the US FDA CFR21 Part 820.30) and how to structure an effective DHF.

Who Should Attend

Aimed at development, quality engineering and regulatory compliance professionals responsible for the development, management and update of the Design History File. This course will be of particular value to professionals involved in the retrospective build of Design History documentation.

Course outline

This is a new course offering for Medical Devices and part of our Qualified Person programme for Medical Devices.

For more information please call our team on +441142 541270. E-mail our training and education team at: [email protected]

Venue

Manchester - Venue to be confirmed

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Tutors

The tutors for this course are as follows:

• Duncan Keeble
• Marcus Orton

• 

  James Pink
  Medical Devices, Vice President
  

  • [email protected]
  • +44 (0) 1143 600868

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