When: 6-8 November 2017
Where: TOPRA, 6th Floor, 3 Harbour Exchange Square, South Quay, London, E14 9GE
What is it?
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This course will cover the following areas:
- Increased Manufacturers obligations
- ISO14155 and the implication of MDR
- Clinical evaluations and investigations
- Post market clinical obligations and studies
- The device life-cycle
- Global strategy requirements
- Pre-clinical evaluation of medical devices
- Medical Device Regulation 2017/745
- Increasing obligations for manufacturers: impact on industry (tracing the changes 2.7/1 rev.3 to rev. 4 to MDR
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Who is it for?
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This course is suitable for anyone working in medical device regulation, or individuals involved in this area, who are interested in the implications of combining medical technology and medicines and students completing their MSc in regulatory affairs (Medicines) or (Medical Devices). This will be a valuable course to ensure you are up to date with the current legislation and guidelines.
This course is now a Credit Bearing Short Course. This means that you can choose to complete the coursework and register onto the TOPRA MSc programme in February 2018. Please contact Kay for more information.
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How do I apply?
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Course fees:
| Type |
Student |
Non-Student |
| Standard |
£1500+VAT |
£1700+VAT |
Discounted places
A limited number of discounted places are available for those working in regulatory agencies, government bodies, charities or patient groups . Please email us for a discount code before making your booking.
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All fees are shown in Pounds Sterling. Terms and conditions apply. Those working for regulatory or government agencies, academic institutions, charities, patient groups or in full time education may be eligible for a discount. To see if you are eligible, For a discount please email us for the code.