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You must get permission to export certain drugs and medicines.
How to carry out a risk assessment if you are applying for a bespoke permit that includes discharging hazardous chemicals and elements to surface water.
Using an ecological momentary assessment to evaluate your digital health product.
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
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.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
The National Treatment Agency for Substance Misuse (NTA) was established in 2001 to improve the availability, capacity and effectiveness of drug treatment. It became part of Public Health England in 2013.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
This series brings together all documents relating to alcohol and drug statistics.
Check what side effects people have reported when they've taken a medicine.
How the MHRA makes decisions on what is a medicinal product (borderline products).
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