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Register to vote Register by 18 June to vote in the General Election on 4 July.
Comply with good pharmacovigilance practice and prepare for an inspection.
Information for businesses on how to comply with consumer protection law on online reviews and endorsements.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
A clampdown on fake reviews and hidden fees has been announced by the Government which will help customers cut the costs of living.
How to use a quasi-experimental study to evaluate your digital health product.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Resources to help anyone developing or running a digital health product to conduct an evaluation.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Understand the approach HMRC uses to work with large business customers.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
The Rapid Review Panel (RRP) assesses innovative infection prevention and control products, equipment and materials for potential use in the NHS.
Anti-choking devices are intended to alleviate choking incidents after Basic Life Support protocols have been attempted and failed. There are numerous counterfeit and unbranded anti-choking devices being sold in the UK online which do not have a valid UKCA or...
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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