Latest News
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17 June 2013
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For years, regulators around the globe have been touting the challenges and benefits of globalization, explaining that a globally diverse product supply chain means needing to rely on regulatory
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Regulatory Update
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7 June 2013
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The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has announced that four National Health Service hospitals have agreed to pilot a new tracking system for high risk medical devices.
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Regulatory Update
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6 June 2013
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A new report by Sweden’s Medical Products Agency and the National Board of Health and Welfare recommends that breast implants manufactured by now-defunct French manufacturer Poly Implant Prothèse
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Latest News
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18 April 2013
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UK regulators said Wednesday that they had, for the first time ever, gotten a man sentenced to prison for his role in falsifying pre-clinical data that was meant to support the regulatory approval of
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Latest News
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12 April 2013
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The UK's Medicines and Healthcare products Regulatory Agency (MHRA) has announced a new set of lofty goals that it says will catapult the regulator to the top tier of those now on the "world
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Regulatory Update
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20 March 2013
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The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has announced that the National Institute for Biological Standards and Control (NIBSC) and the Clinical Practice Research Datalink
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Regulatory Update
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13 March 2013
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The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has announced that it plans to implement new software designed to facilitate its risk-based approach to conducting medicines-related
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Latest News
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12 March 2013
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UK regulators say they plan to launch an "Innovation Office" to assist the regulatory process, and particularly for those companies developing innovative medicines and devices that need the most help
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Latest News
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19 February 2013
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UK regulators sent out a warning to the public on 19 February 2013 regarding what they said was the potential for consumers to be poisoned by unlicensed Chinese medicines imported into the country.At
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Latest News
Regulatory Update
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6 February 2013
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The UK Medicines and Healthcare products Regulatory Agency (MHRA) has submitted recommendations to the European Commission to amend the recently implemented EU pharmacovigilance legislation. In a
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