Research and Markets (http://www.researchandmarkets.com/research/lx3flt/clinical_trial)
has announced the addition of the "Clinical
Trial Regulatory & Guideline Requirements - Including an Update on the
New Clinical Trial Regulation" conference to their offering.
2 & 3 October 2014 - The Rembrandt Hotel, London
The EU Clinical Trials Regulation was finalized and published in the
Official Journal of the EU in May 2014 and is due to come into force in
2016. This new Regulation will replace the European Clinical Trials
Directive (2001/20/EC). This course will provide an essential
understanding to help with compliance for clinical trials, particularly
carried out in the EU.
This course will take you through th regulatory and guideline
requirements for clinical research in Europe, including the new Clinical
Trial Regulation and existing Directive requirements. The key US
requirements which impact on trials being carried out in Europe will
also be covered.
Attending this course will help ensure you are familiar with the
regulations for running clinical trials and with these recent
requirements. The course will highlight the most important of these key
requirements and changes and how these are likely to impact on trials
now and in the future for both Biopharmaceutical companies and study
sites. Regulatory inspectors expect those involved in clinical trials to
be aware of the regulations for controlling clinical trials - this
essential course will also be ideal for this.
For more information visit http://www.researchandmarkets.com/research/lx3flt/clinical_trial
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