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Register to vote Register by 18 June to vote in the General Election on 4 July.
You must get permission to export certain drugs and medicines.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
The following detailed requirements shall apply to veterinary medicinal products other than biological veterinary medicinal products, except where otherwise set out in Section IV.
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.
Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
How the MHRA makes decisions on what is a medicinal product (borderline products).
Register as a manufacturer, importer or distributor of active substances.
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 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.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
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