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Reports, analysis and official statistics
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Data, Freedom of Information releases and corporate reports
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
This guidance demonstrates stakeholders, including the government, working together to address supply issues.
Ten guiding principles that can inform the development of Good Machine Learning Practice (GMLP).
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Guidance following recommendations from the Commission on Human Medicines.
The regulations about working in any healthcare role, and how to register with the appropriate accredited bodies.
Checklists providing a practical guide to using medical devices.
Guidance on prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
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.
Guidance on what pharmacovigilance is and compliance issues from previous inspections.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Guidance on licencing and best use of radiopharmaceuticals and sealed radioactive sources in diagnosis, treatment or research.
Comply with good pharmacovigilance practice and prepare for an inspection.
Guidance for industry on flexible approaches we are taking on good distribution practices.
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