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Guidance for industry on flexible approaches we are taking on good distribution practices.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Provides guidance on making effective use of land, including planning for higher density development.
Information for patients, healthcare professionals and developers of new medicines
Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Find out about clearance applications and how to apply to HMRC for advance confirmation of an exempt distribution when a company purchases its own shares.
Advice on writing clear notices and maximising replies to your FSNs.
How to use a multiphase optimisation strategy (MOST) to evaluate your digital health product.
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