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Register to vote Register by 18 June to vote in the General Election on 4 July.
The Charity Commission is seeking your views on the charitable status of complementary and alternative medicines.
The Commission on Human Medicines (CHM) advises ministers on the safety, efficacy and quality of medicinal products. CHM is an advisory non-departmental public body, sponsored by the Department of Health and Social Care .
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
How to conform with the legal requirements for placing medical devices on the market.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
Who you should contact if a pet or other animal or human has an unexpected reaction to a veterinary medicine or a problem with a microchip
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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