ENT, Ophthalmology & Skin Medicines/Medical Devices

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                    "description": "(a) Potential Framework Participants must be able to confirm supply of ENT, Ophthalmology & Skin Medicines holding a current and valid UK Marketing Authorisation that has been approved by the MHRA or EMEA (European Medicines Agency) market authorisation at the date of the tender submission for all Medicines tendered. (b) Potential Framework Participants and any sub-contractor(s) must possess valid certification of BS EN ISO 9001 or equivalent. (c) All tendered Goods must comply with the MHRA best Practice Guidance on Labelling and Packaging and the National Patient Safety Agency (\"NPSA\") Guidelines on Packaging and Labelling on pack design. (d) Potential Framework Participants must be able to confirm that any products submitted and classed as Medical Devices carry CE declaration of conformity at the date of the tender submission for all Medical Devices tendered.",
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