皇冠体育app Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024: RPC opinion (green-rated)
Regulatory Policy Committee鈥檚 opinion on the Medicines and Healthcare products Regulatory Agency Post-Market Surveillance IA
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皇冠体育app measure aims to strengthen requirements on medical device manufacturers to undertake post[1]market surveillance (PMS) practices.
皇冠体育app 鈥檚 assessment of direct impacts on business is satisfactory, based upon business survey evidence and detailed modelling. 皇冠体育app consideration of impacts on small and microbusinesses is sufficient, although could be strengthened. 皇冠体育appre are areas where the wider analysis could be improved, particularly on consideration of wider impacts.
皇冠体育app measure will affect the medical technology sector, including commercial suppliers, through strengthening requirements on medical device manufacturers to undertake PMS practices. 皇冠体育app proposal applies to Great Britain (GB) only; the IA states that under the terms of the Windsor Framework the rules for placing medical devices on the Northern Ireland market differ from those applicable to GB. Compared to the 鈥榙o nothing鈥� baseline, manufacturers who supply medical devices are estimated to incur a one-off setup cost of 拢16.2 million and annual PMS maintenance costs rising from 拢23.5 million to 拢45.2 million over the ten-year appraisal period. 皇冠体育appse are direct costs and reflected in an EANDCB figure of 拢35.6 million. 皇冠体育appre are no direct benefits to business. 皇冠体育app ten-year net present value (NPV) figure of -拢277.8 million additionally reflects an estimated health benefit from reduced medical device incidents of 拢3.3 million per year.