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Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to use evidence of drug-related activity and harm to improve prevention and treatment of substance misuse and associated problems.
This guidance explains the legal framework for labelling and packaging as described in UK legislation and gives best practice for producing medicines labelling and packaging.
This guidance demonstrates stakeholders, including the government, working together to address supply issues.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Comply with good pharmacovigilance practice and prepare for an inspection.
Guidance on what pharmacovigilance is and compliance issues from previous inspections.
Guidance following recommendations from the Commission on Human Medicines.
How to register veterinary practice premises for vets to be able to supply veterinary medicines and inspection issues.
Guidance on licencing and best use of radiopharmaceuticals and sealed radioactive sources in diagnosis, treatment or research.
What is the Financial Remedies Court (FRC) The FRC is a specialist part of the Family Court. Following the breakdown of a marriage or civil partnership there are often financial issues that need to be resolved. Financial support for children...
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Guidance on prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
Links to EU guidance, as it stood immediately before end of transition period.
Keep up to date with the latest information from the UK GLP monitoring authority.
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