TOPRA annual Medical Device and IVD Symposium 2018

Section 1: The Programme and Speakers

It will help considerably in the planning and organisation of our events if you would answer the following questions. Thank you very much.

Question Title

* 1. Which would you consider the most outstanding session for you and why?

TOPRA Annual lecture 2018

Update on progress and preparation for the Medical Device and In Vitro Device Regulations

Gathering clinical evidence, evaluating clinical data and determination of post market clinical follow-up under the MDR

Digital health and the new General Data Protection Regulation (GDPR)

Brexit

Medicinal products with integral medical devices – bringing two worlds together

Developing cooperation at the interface between medicinal products and medical devices

IVD Performance Evaluation Requirements

IVD Technical Documentation Requirements

Please provide more details on why you found this session outstanding - was it the overall session or an individual contributor?

Question Title

* 2. Which would you consider the most useful session for you and why?

TOPRA Annual lecture 2018

Update on progress and preparation for the Medical Device and In Vitro Device Regulations

Gathering clinical evidence, evaluating clinical data and determination of post market clinical follow-up under the MDR

Digital health and the new General Data Protection Regulation (GDPR)

Brexit

Medicinal products with integral medical devices – bringing two worlds together

Developing cooperation at the interface between medicinal products and medical devices

IVD Performance Evaluation Requirements

IVD Technical Documentation Requirements

Please provide more details on why you found this session useful - was it the overall session or an individual contributor?

Question Title

* 3. Which would you consider the least useful session for you and why?

TOPRA Annual lecture 2018

Update on progress and preparation for the Medical Device and In Vitro Device Regulations

Gathering clinical evidence, evaluating clinical data and determination of post market clinical follow-up under the MDR

Digital health and the new General Data Protection Regulation (GDPR)

Brexit

Medicinal products with integral medical devices – bringing two worlds together

Developing cooperation at the interface between medicinal products and medical devices

IVD Performance Evaluation Requirements

IVD Technical Documentation Requirements

Please provide more details on why you found this session least useful - was it the overall session or an individual contributor?

Question Title

* 4. Can we improve on anything? Please detail

Question Title

* 5. Did you find the extra IVD parallel sessions a useful alternative stream to the MDD sessions

Yes

Question Title

* 6. Did you attend any of the parallel sessions on CMC, ATMP, CT, PI's ?

Yes

Was not aware of parallel sessions

Question Title

* 7. Did you attend of any of the Professional Competence sessions ?

Yes

I was not aware of the Professional Development sessions

Which topics did you feel were especially valuable or would you like to see included in the future?

Question Title

* 8. How useful was the pullout programme in your delegate badge?

Very useful

Useful

Not practical

Did not use it

Question Title

* 9. How would you rate the online programme at www.toprasymposium.org?

Very useful

Useful

Not practical

N/A – did not access it