{"product_id":"medical-devices-policy-suite","title":"Medical Devices Policy Suite (UK MDR 2002 | MHRA | PUWER 1998 | LOLER 1998 | CQC Reg 12, 15)","description":"\u003cp\u003eComplete CQC-compliant Medical Devices documentation suite. Policy Template (MDV1), Excel Workbook (MDV2), Word Forms (MDV3), Master Checklist (MDV5). Forms: Medical Device Register, MHRA Field Safety Notice Tracker, Adverse Event Reporting (Yellow Card), Equipment Inspection \u0026amp; Servicing Log, PUWER\/LOLER Compliance Checks, Decontamination Record, Staff Competency Assessment, Training Record, Quarterly Audit. Regulatory: UK MDR 2002; MHRA; PUWER 1998; LOLER 1998; CQC Reg 12, 15.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003e£49.99 one-time purchase.\u003c\/strong\u003e ISO 9001 + ISO 45001 certified.\u003c\/p\u003e","brand":"Hiscock \u0026 Co — Regulatory Compliance","offers":[{"title":"Default Title","offer_id":57324368626008,"sku":"MDV-v3-2","price":49.99,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0984\/5008\/0088\/files\/MDV_Product_Cover.png?v=1779210799","url":"https:\/\/hiscockco.co.uk\/products\/medical-devices-policy-suite","provider":"HISCOCK \u0026 CO Regulatory Compliance","version":"1.0","type":"link"}