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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
Use this form to transfer a product licence, also known as a marketing authorisation, to a different owner.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
An initiative for companies committed to integrating 10 corporate responsibility principles in their business operations and strategies.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
Guidance on the submission, processing and assessment of all completed paediatric studies sponsored by Marketing Authorisation Holders (MAHs)
The CMA is investigating the partnership between Microsoft Corporation (Microsoft) and Mistral AI.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Form L7 for the isolation, identification and toxin detection of clostridium botulinum and Staphylococcus aureus.
VICH consultation until 15 August 2024 on guidelines relating to the technical requirements for demonstrating pharmaceutical development of veterinary medicinal products.
Remedies form to be completed by merger parties for proposing remedies during a phase 2 merger inquiry.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Volume 37 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Sets out legal text on the manufacture, authorisation, marketing, distribution and post-authorisation surveillance of veterinary medicines.
Volume 8 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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