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Check what you need to do to sell cosmetic products in Great Britain.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to use a before-and-after study to evaluate your digital health product.
Get a free permit to join family from the EU, Switzerland, Norway, Iceland or Liechtenstein in the UK - check if you’re eligible, documents you need to apply.
How to use a quasi-experimental study to evaluate your digital health product.
Publish your code and use open source to improve transparency, flexibility and accountability.
Good Practice Guide (GPG) 45 helps you decide how to check someone's identity.
What you need to know about and do to comply with the law and keep consumers safe.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
You can make observations on the patentability of a published patent application.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How the protected online filing (PROOF) scheme can help you prevent fraudulent changes to your company.
How to create a model of how your digital health product works and choose measures for your evaluation.
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.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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)’
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