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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Guidance for business and government departments.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
How to change the ownership from one marketing authorisation (MA) holder to another.
Guidance on making a disclosure protected by the Public Interest Disclosure Act 1998, (whistleblowing) to the Certification Officer
Information on how to revalidate a UK CoC (and UK GMDSS at the same time).
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Disclosure of the identity of individuals making applications and complaints to the Certification Officer
How to check if the organisation giving you an award is registered and accredited by the exams regulator
The CMA investigated alleged excessive and unfair pricing, anti-competitive agreements and abusive conduct with respect to hydrocortisone tablets under Chapters I and II CA98 and Articles 101 and 102 TFEU.
Reports of investigations into the financial affairs of trade unions. All decisions are in PDF format.
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Apply for a higher education course, track your application and accept or reject your offers.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to make sure an application relating to an authorisation for a veterinary medicine is complete and will pass validation.
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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