Wed 29 Feb 2012
A one day training course
Who should attend?
This course is for all clinical research professionals in the non-commercial sector working on trials subject to inspection by the Medicines and Healthcare Products Regulatory Agency (MHRA).
Course Structure
The morning session will concentrate on issues and systems at an organisational level from within the R&D department together with a practical exercise looking at the steps and inputs needed when preparing your GCP Inspection Dossier. The afternoon will drill down further to focus on issues relevant at the trial site level including the key departments of pharmacy and clinical laboratory.
Course Date
The one day course is currently being held on 29 February – London
Further details in the attached pdf and on the event web page: http://www.rdforum.nhs.uk/004c.asp?entryid=984 or click here to download the PDF.
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