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Register to vote Register by 18 June to vote in the General Election on 4 July.
Competent authorities of exporting countries should use the relevant model health certificate as a template to create a version exporters can apply for to export other animal by-products to Great Britain, the Channel Islands or Isle of Man.
Compare different evaluation approaches and choose an appropriate method.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
How to use a cost effectiveness analysis to evaluate your digital health product.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
FCDO travel advice for Germany. Includes safety and security, insurance, entry requirements and legal differences.
Guidance on choosing evaluation study types and methods.
How to write up and share your findings
How to use a cost utility analysis to evaluate your digital health product.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
PHE's Centre for Radiation, Chemical and Environmental Hazards provides radiological protection advice, services and training.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
How to use a cost benefit analysis to evaluate your digital health product.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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