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Register to vote Register by 18 June to vote in the General Election on 4 July.
Waste electrical and electronic equipment (WEEE) - retailer and wholesaler responsibilities, waste collection and compliance schemes.
How to use a cost utility analysis to evaluate your digital health product.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Information for manufacturers, healthcare professionals, researchers and patients on software as a medical device (SaMD) and AI as a medical device (AIaMD).
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
What to do if a laptop or tablet you’ve received from a DfE programme is not working.
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Further documents relating to the Medicines and Medical Devices Bill 2020.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
Requirements for Immunological Veterinary Medicinal Products.
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