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Data, Freedom of Information releases and corporate reports
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to change the ownership from one marketing authorisation (MA) holder to another.
How the Certification Officer (CO) applies her powers to act without a complaint to conduct investigations into trade unions and employers’ associations.
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
How to renew marketing authorisations for products granted through different routes and at different times.
Certification Officer (CO) decisions made in response to complaints and applications.
How to apply for authorisation to become a regulated claims company, understanding the fee structure, and how and when to pay fees.
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
How someone in Poland can get documents prepared, witnessed or certified, take an oath of British citizenship and obtain informative notes.
The CMA is investigating whether ESS might be abusing a dominant position in the supply of management information systems (MIS) software by making it difficult for schools to switch provider.
We have increased the checks on addresses provided in trade mark applications and introduced a process for reporting misconduct by unregulated agents.
A list of MCA Clients and certificates currently in force
Designs correction of error notices are used to notify any third party of a proposed correction of a clerical error made by the registry prior to a correction taking place.
The CMA investigated alleged excessive and unfair pricing with respect to liothyronine tablets under Chapter II CA98.
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