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Register to vote Register by 18 June to vote in the General Election on 4 July.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
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.
Answers to frequently asked questions on Approved Document B including 2020 and 2022 amendments.
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
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).
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
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
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
What an SIA approved contractor must do to remain approved.
Submission dates and how the submissions using the EC decision reliance procedure work.
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
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to get relief from excise duty on oil used in certain ways using the Industrial Relief Scheme, also known as the Tied Oils Scheme.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Information for NHS trusts on the Crown Commercial Service (CCS) health temporary staff frameworks approved by NHS Improvement.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
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