Drug Regulatros, MHRA, Publish Comment on Voluntary parallel scientific advice with NICE and the MHRA

Drug Regulatros, MHRA, Publish Comment on Voluntary parallel scientific advice with NICE and the MHRA

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The MHRA have been in discussion with the National Institute for Health and Clinical Excellence (NICE) about the possibility of running voluntary parallel scientific advice in relation to clinical trial programmes and have agreed to undertake a small pilot commencing March 2010.

Companies who are interested in being considered for this pilot should already have experience of MHRA and NICE scientific advice procedures for other products and should contact Ian Hudson at MHRA – ian.hudson@mhra.gsi.gov.uk – or Carole Longson/Seren Phillips at NICE.

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Damien Bové is the drug development and regulatory consultant (pharmaceutical or biotechnology), I work with my clients to define a drug development target, define a drug development strategy, define a regulatory strategy or define a commercial strategy. Our clients are generally raising funds or looking to license out their technology and we help them achieve it. If you want to know more don’t hesitate to get in touch.


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Sign up for the most value add free newsource you can get for free. We spend a huge amount of time and effort monitoring the main drug / device regulators websites for changes in the regulatory environment, and capture between 20 and 40 new regulations, rules and initiatives each month, and summaries them in a fantastic FREE monthly Regulatory and Market Round Up. You can Un-Subscribe at any time and we don not share your details with anybody. You can’t afford to miss out on this service. Just fill in the form below.

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