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How to spot Batrachochytrium salamandrivorans, what to do if you suspect it and measures to prevent its spread.
Use a separate statement of objection form for each Japanese GI product name you object to.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
Sets out COVID-19 testing for hospice patients and staff.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Find details of recent trade mark applications or amendments by searching the journal
Volume 38 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
This is a work sharing model for the co-ordinated assessment of a generic application that has been filed with multiple Access Consortium agencies.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Volume 31 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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