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Links to EU guidance, as it stood immediately before end of transition period.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Guidance for industry on flexible approaches we are taking on good distribution practices.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This guidance is intended to support billing authorities in administering the 2024/25 Retail, Hospitality and Leisure Business Rates Relief Scheme.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Comply with good pharmacovigilance practice and prepare for an inspection.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
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.
Legal requirements and good practice guidance for Veterinary Practice Premises Inspections.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
We are producing guidance and information for industry, healthcare professionals and patients covering the coronavirus (COVID-19) outbreak.
Guidance for prescribing vets on the use of the cascade.
Guidance primarily aimed at local responders covering some humanitarian issues that may arise during the recovery phase of an emergency in the UK.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
How to claim the new merged scheme R&D expenditure credit (RDEC) and enhanced R&D intensive support for accounting periods beginning on or after 1 April 2024.
How to apply for a traditional herbal registration (THR) to market a herbal medicine in the UK.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
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