Regulatory Affairs Working Party Seminar 2022 Feedback Survey

Thank you for attending our Regulatory Affairs Seminar. We hope that you found the seminar informative and worthwhile. 
 
To assist us in improving our service to you would it be possible for you to complete the survey below. 

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* 1. Please give your assessment of the standard and content of the presentations at BIVDA's Regulatory Affairs Seminar 2023:

  Poor 1 2 3 4 Excellent 5
Session 1 - MHRA Software Roadmap
Johan Ordish, MHRA
Session 2 - IVD Roadmap / UKCA
Ashleigh Batchen, BIVDA / Tom Beale, Agilent
Technologies / Camilla Fleetcroft
Session 3 - MDCG Roadmap
Andrew Rutter, QuidelOrtho
Session 4  - Class D IVDs: what do you need to do?
Erica Conway, MCRA
Session 5 – BSI Standards
Rob Turpin, BSI
Session 6 – The US Regulatory Process
Stuart Angell, IVDeology

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* 2. Were the presentations detailed enough?

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* 3. Did you find the seminar relevant to your needs?

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* 4. Any other comments about the content?

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* 5. Are there any other topics you would like to have covered or dealt with more fully?

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* 6. Please give us your assessment of whether the presentations were useful and of the way they were presented.

  Poor 1 2 3 4 Excellent 5
Usefulness
Presentation 

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* 7. Was the seminar efficiently organised?

  Poor 1 2 3 4 Excellent 5
Invitations and information beforehand
On the day

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* 8. Which room layout would you prefer for future seminars?

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* 9. What if anything did you dislike about the seminar?

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* 10. Your details

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