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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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
Find out about the rules for placing transportable pressure equipment on the market in Great Britain from 1 January 2023.
This guidance is for UK Conformity Assessment Bodies (CABs) who are intending to subcontract tasks such as testing, certification or inspection.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
SIA regulation: how the SIA enforces the law and what the penalties are for breaking it.
Licence and registration application information for companies that deal in precursor chemicals.
What you need to know about and do to comply with the law and keep consumers safe.
A Guide for Employers and Employees to the role of the Central Arbitration Committee (CAC) for these regulations
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Pharmacovigilance system requirements
Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
When you can use a designated UK-based conformity assessment body (CAB) to test your goods against the importing market’s regulations.
How to make an origin declaration if you're using it as proof of origin for products using the Developing Countries Trading Scheme.
This series brings together all DWP documents relating to Better Regulation.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
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.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Resources for businesses.
Guidance for business and government departments.
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