Thank you for your participation to the 4th European Conference on Clinical Research in Vienna.

EUCROF is committed to organise informative conferences bringing optimal value to all Clinical Research professionals. As a participant to the recent 4th conference, we value your feed-back giving us the opportunity to better meet or even exceed your expectations in the future.

Please take a couple of minutes to provide your perspective (anonymous) and use free text sections as extensively as you wish:

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* 3. Conference Organization

  Excellent Good Average Poor N/A
Date of the event (i.e. late February)
Conference Website
Registration process
Accommodation
Logistic support before and during the conference
Suitability of the location
Catering
Networking opportunities
Social event (Monday evening)
Staff/organisers

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* 4. Conference Programme

  Excellent Good Average Poor N/A
Business pertinence of topics?
Quality of presentations?
Conference format (plenary / parallel)

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* 5. Sessions
Would your time permit, please further evaluate the Sessions:

Monday
The Key Note speaker lecture - How Did This Happen?
Plenary session

  Excellent Good Average Poor N/A
Presentation content

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* The Clinical Trials Regulation
Plenary session

  Excellent Good Average Poor N/A
Presentation content
Session format

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* The gold sponsor lecture- Latest geographic trends in global industry Clinical trials: who is winning, who is losing?

  Excellent Good Average Poor N/A
Presentation content

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* The New addendum to GCP E6 (R2) & Operating models
Plenary session

  Excellent Good Average Poor N/A
Presentation content
Session format

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* Part 1 -Risk Based approaches in Clinical Trials
Plenary session

  Excellent Good Average Poor N/A
Presentation content
Session format

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* Part 2 - eTMF, eSource, Data Privacy...
Plenary session

  Excellent Good Average Poor N/A
Presentation content
Session format

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* Tuesday
e-Systems and Technical Solutions
Parallel session

  Excellent Good Average Poor N/A
Presentation content
Session format

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* Clinical Trials in Paediatric Population
Parallel session

  Excellent Good Average Poor N/A
Presentation content
Session format

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* EU Medical Device Regulation
Parallel session

  Excellent Good Average Poor N/A
Presentation content
Session format

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* Data Protection Regulation (GDPR) revamped
Parallel session

  Excellent Good Average Poor N/A
Presentation content
Session format

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* Post approval considerations
Plenary session

  Excellent Good Average Poor N/A
Presentation content
Session format

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* Brexit
Plenary session

  Excellent Good Average Poor N/A
Presentation content
Session format

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* Have you any preference for more panel discussions and/or parallel track sessions?

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* What are the topics that you would like to see covered during the next conference?

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* 6. B2B Meetings

  Excellent Good Average Poor N/A
Planning the meetings online
Onsite organisation of meetings

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* Would you be interested in the B2Bs again during the next conference?

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* 7. Your overall conference experience

  Surely Likely Unlikely Don´t know
Would you join again?
Would you recommend this event?

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* 8. What would be the ideal frequency of the conference?

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* 9. Other comments? What should we improve in 2020....

We thank you for your feedback.

The EUCROF Board and Conference Committees

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