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Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
The epidemiology, symptoms, diagnosis and management of Nipah virus infections.
Pharmacovigilance system requirements
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Order birth, adoption, marriage, civil partnership and death certificates from the General Register Office (GRO) - find GRO index numbers
Look up a trade mark to see if something identical or similar to your brand is already registered.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
How to make sure an application relating to an authorisation for a veterinary medicine is complete and will pass validation.
Check what you need to do to employ teachers who are non-UK citizens.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
How to contact MHRA for specific services or enquiries.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Don’t include personal or financial information like your National Insurance number or credit card details.
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