Presentation on what it takes to get a clinical study off the ground in the UK along with some info on the impact of directive 2007/47/EC will have on clinical data requirements
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Clinicals In The Uk 26 January 2009
1. Undertaking a Clinical Study for a Medical Device in the UK Presentation to the UKTI Healthcare Briefing Tour Kevin Webb Head of Regulatory & QA Mediqol Limited
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5. The Medicines and Healthcare products Regulatory Agency (MHRA) is the UK Competent Authority