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Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Find UK trade data from HMRC. Look up data about imports, exports, commodities and traders.
How to make sure an application relating to an authorisation for a veterinary medicine is complete and will pass validation.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Information on how to revalidate a UK CoC (and UK GMDSS at the same time).
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
How to legally run a business that deals with the wholesale of animal medicines (veterinary medicinal products) and the WDA Register.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
British Medical Association trade union: annual returns, rules, statement to members, decisions and other related documents.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Documents, certificates, letters and notes available at British consulates in Armenia.
Check if your import, export or re-export needs a permit or certificate under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
How to change the ownership from one marketing authorisation (MA) holder to another.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How to check if the organisation giving you an award is registered and accredited by the exams regulator
Guidance for the pharmaceutical industry on who can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
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