An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT...

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An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection Service

Transcript of An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT...

Page 1: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

An agency of the European Union

Training session for Stakeholders

•Clinical Trial Results in EudraCT V10

Presented by: Noemi ManentCompliance and Inspection Service

Page 2: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

Agenda

Purpose

Legal basis requirements

Clinical Trial Results in EudraCT V10

Q&A

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Page 3: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

Legal basis requirements

Press release issued on 19 June 2014, the official date of the end of the programming of EudraCT has been announced 21 July 2014 . The posting of summaries of clinical study results in the European Clinical Trials Database (EudraCT) becomes mandatory for Sponsors as of 21 July 2014.

This date corresponds to the finalisation of the programming of the database as referred to in a European Commission guideline on results related information (2012/C 302/03).

Press release:

http://www.ema.europa.eu/ema/index.jsp?curl=pages/news_and_events/news/2014/06/news_

detail_002127.jsp&mid=WC0b01ac058004d5c1

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Page 4: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

Training session - CT Results in EudraCT V10

Few examples are already available in the public domain:

structured data set

attachment

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Page 5: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

Results in EudraCT V10

Results are provided for the trial and not per CTA

There are three status for results in EudraCT

draft (the user is preparing the results in the system)

posted (the user has satisfactorily validated the results and agreed with the T&C for publication)

finalised (the results are final and can be viewed on the EU CTR if the protocol related records are published)

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Page 6: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

Results in EudraCT V10 draft (the user is preparing the results in the system)

preliminary and can change at any time.

posted (the user has satisfactorily validated the results and agreed with the T&C for publication)

The data / document format have been validated against the system validation rules established and available on the EudraCT website

The sponsor has agreed with the T&C for publication

There is a delay of 14 days between the posting date and the publication date

During this period, the sponsor has the possibility to retract the publication. If so, the results status returns to “draft”.

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Page 7: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

Results in EudraCT V10

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Page 8: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

Results in EudraCT V10

Finalised:

the results are final and can be viewed on the EU CTR if the protocol related records are published.

Cases when the results are not published:

Phase 1 trials conducted in adults (not part of a PIP)

If all CTAs related to the trial have the CA decision/IEC opinion missing

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Page 9: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

Results in EudraCT V10

The results can be presented as follows:

With an attachment only (PDF…): option reserved for old trials (that do not included paediatrics population) that have ended in the past on or before 21 July 2013

with structured data (with or without attachment):

trials that have ended after 21 July 2013 (less than a year before the finalisation of EudraCT)

Trials that include paediatric population (even if they have ended in the past)

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Page 10: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

Clinical Trial Results – training Environment

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Page 11: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

EudraCT Result training environment

Presentation title (to edit, click View > Header and Footer)11

Page 12: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

Your page

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Page 13: An agency of the European Union Training session for Stakeholders Clinical Trial Results in EudraCT V10 Presented by: Noemi Manent Compliance and Inspection.

EudraCT Result training environment

• Launched in August 2014

• URL link available on the EudraCT public website

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