Difference between revisions of "EMEA - EudraCT"
| Line 1: | Line 1: | ||
Here are some documents as background information: | Here are some documents as background information: | ||
| − | The following link defines the legal framework for establishing EudraCT: | + | The following link defines the legal framework for establishing EudraCT: |
| − | |||
http://ec.europa.eu/enterprise/pharmaceuticals/clinicaltrials/clinicaltrials_en.htm | http://ec.europa.eu/enterprise/pharmaceuticals/clinicaltrials/clinicaltrials_en.htm | ||
Revision as of 22:28, 12 December 2009
Here are some documents as background information:
The following link defines the legal framework for establishing EudraCT: http://ec.europa.eu/enterprise/pharmaceuticals/clinicaltrials/clinicaltrials_en.htm
EudraCT can be found here: https://eudract.emea.europa.eu/
You have our data dictionary above, which is derived from the Clinical Trial Application form. The latest version of which will be used for Version 8 of EudraCT can be found here: http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol-10/application-form2009.pdf
In version 8 we will be making part of the information contained in the EudraCT system available to the public in accordance with the following guidelines and lists of data fields.
Guideline for "Article 57" trials "Communication from the Commission regarding the guideline on the data fields contained in the clinical trials database provided for in Article 11 of Directive 2001/20/EC to be included in the database on medicinal products provided for in Article 57 of Regulation (EC) No 726/2004". (2008/C 168/02) http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol-10/2008_07/c_16820080703en00030004.pdf
Associated with this guideline is the list of data fields to be made public. "List of fields contained in the 'EudraCT' clinical trials database to be made public, in accordance with Article 57(2) of Regulation (EC) No 726/2004 and its implementing guideline 2008/C168/02 (February 2009)". http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol-10/2009_02_04_guideline.pdf
Guideline for paediatric trials "Communication from the Commission - Guidance on the information concerning paediatric clinical trials to be entered into the EU Database on Clinical Trials (EudraCT) and on the information to be made public by the European Medicines Agency (EMEA), in accordance with Article 41 of Regulation (EC) No 1901/2006". (2009/C 28/01) http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol-10/2009_c28_01/2009_c28_01_en.pdf
Associated with this guideline is the list of data fields to be made public. "List of fields to be made public from EudraCT for Paediatric Clinical Trials in accordance with Article 41 of Regulation (EC) No 1901/2006 and its implementing guideline 2009/C28/01 (February 2009)". http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol-10/2009_02_04_guideline.pdf
We will also be collecting information on Paediatric clinical trials conducted in third countries (i.e. outside of the EU/European Economic Area(EEA)) that form part of a Paediatric Investigation Plan (PIP) (paediatric clinical trials with sites inthe EU/EEA are already included)
You will also find the Business Use Cases that are relevant to the Version 8 release of EudraCT. These may help in understanding the processes that we are implementing and again you may share them on the wiki.
List of Fields Contained in the EUDRACT Clinical Trials Database
Paediatric clinical trials to be entered into the EU Database on Clinical Trials (EudraCT)
