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What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Check the tariff classification for a defined daily dose of active substances.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Information on the large programme uplift, which applies to high quality, larger study programmes that provide students with additional stretch and challenge.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Explanation of terms used in Ofsted's official and national statistical releases.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
The way you apply to licence biological products has changed
Information for post-16 providers on the next steps towards delivery of T Levels.
Find out which types of food are zero-rated and which are standard-rated for VAT purposes.
Development of the ENhancing Assessment of Common Therapeutic factors (ENACT) rating scale
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 the MHRA makes decisions on what is a medicinal product (borderline products).
Information for post-16 institutions considering expressing an interest to deliver the first 3 T levels in 2020 to 2021 academic year.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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