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What we check and how you apply for approval.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
Find out if you need to apply for an approval check, how to apply and how HMRC will carry out the checks as part of the business registration process.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
How to set up and run a motorcycle approved training body (ATB) to provide compulsory basic training (CBT) and the direct access scheme (DAS) to learner riders
Using an ecological momentary assessment to evaluate your digital health product.
How to choose an SIA approved contractor and why you should.
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
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance on the examination stage for Nationally Significant Infrastructure Projects.
What an SIA approved contractor must do to remain approved.
How to apply for repayment of import duty and VAT on protective equipment or medical supplies brought into the UK from non-EU countries from 30 January 2020 up to 31 December 2020.
Submission dates and how the submissions using the EC decision reliance procedure work.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Apply for a High Potential Individual (HPI) visa if you've been awarded a qualification by an eligible university in the last 5 years - eligibility, fees, documents, switch, bring your partner and children
Answers to frequently asked questions on Approved Document B including 2020 and 2022 amendments.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Apply to become or identify an approved manufacturer authorised to carry out conformity assessment.
Apply to be a waste electrical and electronic equipment (WEEE) producer compliance scheme and operate legally under your approval.
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