Transcription of Reflection Paper Risk-Based Quality Management Clinical …
{{id}} {{{paragraph}}}
Example: stock market
Reflection Paper Risk-Based Quality Management Clinical …
18 November 2013 EMA/269011/2013 Compliance and Inspection Reflection Paper on risk based Quality Management in Clinical trials Draft Agreed by the Clinical Trial Facilitation Group (CTFG) for release for consultation 31 May 2011 Draft Adopted by the Good Clinical Practice (GCP) Inspectors Working Group for consultation 14 June 20111 Start of public consultation 5 August 2011 End of consultation (deadline for comments) 15 February 2012 Agreed by the Clinical Trial Facilitation Group (CTFG) for publication 13 September 2013 Adopted by GCP Inspectors Working Group 12 September 2013 Keywords Quality Management , Risk Management , Quality Tolerance Limit, Risk Control, Clinical Trial 7 Westferry Circus Canary Wharf London E14 4HB United Kingdom An agency of the European Union Telephone +44 (0)20 7418 8400 Facsimile +44 (0)20 7418 8416 E-mail Website European Medicines Agency, 2013.
intervals the progress of a clinical trial, the safety data, and the critical efficacy endpoints, and to recommend to the sponsor whether to continue, modify, or stop a trial. 4. Electronic data capture (EDC) A system that allows collecting clinical trial data in electronic form and importing them without the use of paper.
Tags:
Information
Domain:
Source:
Link to this page:
Please notify us if you found a problem with this document: