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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.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
Find out how you can set up a producer organisation (PO) as a group of growers.
What you need to know about and do to comply with the law and keep consumers safe.
UK guideline on GMP for decentralised manufacturing, ensuring compliance with EU GMP principles for safe, quality medicinal products.
How regulators determine fit and proper person status when you apply for approval as a compliance scheme or accreditation as a reprocessor or exporter.
You can claim a relief to pay no Customs Duty and VAT if you're importing inherited goods into the UK.
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