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Find out how to account for VAT schemes on business gifts, samples and promotional schemes.
Submission dates and how the submissions using the EC decision reliance procedure work.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
This guidance provides details of the PAR changes we have made for these funds, giving more flexibility to councils to change projects.
This guidance is designed to help UKHSA customers and partners to navigate engaging and working with us and to signpost upcoming events and opportunities.
HMT management information about the Coronavirus Business Interruption Loan Scheme (CBILS), Coronavirus Large Business Interruption Loan Scheme (CLBILS), Bounce Back Loan Scheme (BBLS) and Future Fund Scheme.
Outlines the provisions of the Food (Promotion and Placement) (England) Regulations 2021, and provides assistance in understanding and applying them.
Documents relating to the Changing Futures programme.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Marketing authorisations granted in 2024
How the MHRA processes variations to Marketing Authorisations (MAs)
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
The biggest ever drive to help employers unlock the talent across Britain will be at the heart of a new Government campaign to create the workforce of the future, the Work and Pensions Secretary unveiled today.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
How to get plant breeders' rights and what protection it gives your plant varieties.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Pharmacovigilance system requirements
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