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Read about businesses that have participated in support schemes funded by the UK government.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
The Committee on Mutagenicity of Chemicals in Food, Consumer Products and the Environment (COM) assesses and advises on mutagenic risks to humans. COM is an advisory non-departmental public body, sponsored by the Department of Health and Social Care and the...
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
The Traffic Commissioner for London and the South East's written decision for Hi-Stanford Scaffolding Ltd (OK2042641)
Find details of recent trade mark applications or amendments by searching the journal
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Your chances of obtaining a useful patent are significantly greater if you use an attorney. A patent specification is a legal document and requires specialist skills to draft properly.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Information for people who wish to apply to release a vaccine or a blood product to market in the UK.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Examples of unacceptable trade marks around protected emblems, internet domain names and your company name.
This is a work sharing model for the co-ordinated assessment of a generic application that has been filed with multiple Access Consortium agencies.
Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Information on how UK companies can control risks when doing business in Mexico.
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