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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
RA1, RA2, RA3, RA4, RA5 bilingual forms for completion following a drugs test in custody.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Information about the EU Regulations and their implementation in Northern Ireland
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
The process for applicants applying for a paediatric investigation plan (PIP) modification or waiver.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
What packaged goods are, how they are labelled, units of measurements used and compliance with weights and measures regulation.
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