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Register to vote Register by 18 June to vote in the General Election on 4 July.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
How developers can create and enhance habitat off-site or buy biodiversity units to achieve biodiversity net gain (BNG).
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Pharmacovigilance system requirements
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Find out how to apply VAT to charges for postage, delivery services and how to treat direct marketing services involving distribution of printed matter.
How veterinary medicines can be advertised.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
How to renew marketing authorisations for products granted through different routes and at different times.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
How to apply for marketing authorisation via this new procedure.
Decisions made by MHRA on adverts reported to have breached the legislation on advertising medicines.
What happens when Rural Payments Agency field officers visit your holding, including checks on tagging, holding registers and movement records.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Comply with good pharmacovigilance practice and prepare for an inspection.
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