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The MHRA is ready to provide any assistance for clinical trials applications submitted for COVID-19
Information and guidance on a range of medical devices for users and patients.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for 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.
How to get an ENG1 or ML5 medical certificate.
Actions that trial sponsors should consider to build resilience into clinical trial design
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
How to meet the good clinical practice standards for clinical trials and what to expect from an inspection.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
The Vaccine Development Evaluation Centre (VDEC) at Porton Down in Wiltshire facilitates the development and evaluation of new vaccines and therapeutics.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Explanation of terms used in Ofsted's official and national statistical releases.
How the MHRA makes decisions on what is a medicinal product (borderline products).
These terms and conditions set out the requirements of membership of the Secretary of State for Transport’s Honorary Medical Advisory Panels.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
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