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Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
How OPSS contributes to international legal metrology and who to contact.
This is a work sharing model for the co-ordinated assessment of a generic application that has been filed with multiple Access Consortium agencies.
This guidance sets out how the MHRA is handling centralised applications that were still pending on 1 January 2021.
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.
FDA trade union: trade union: annual returns, rules, statement to members, decisions and other related documents.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Guidance on how the Certification Officer Intends to use these Powers
Guidance for the pharmaceutical industry on who can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Apply for a higher education course, track your application and accept or reject your offers.
Service for Marketing Authorisation Holders, Manufacturers and Wholesalers.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
How ship owners, brokers and operators can apply to MCA for passenger, bunker, tanker and wreck removal compulsory liability insurance certificates
The Royal Mint (RM) is the world’s leading export mint, making coins and medals for an average of 60 countries every year. However, its first responsibility is to make and distribute United Kingdom coins as well as to supply blanks...
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to legally run a business that deals with the wholesale of animal medicines (veterinary medicinal products) and the WDA Register.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Information about what to do if you receive a warning or advisory letter from the CMA.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Documents relating to workforce management information summary data for the Competition and Markets Authority.
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