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Check the tariff classification for flavour pods.
For manufacturers of long-term samplers and test laboratories who carry out testing of equipment.
UK guideline on GMP for decentralised manufacturing, ensuring compliance with EU GMP principles for safe, quality medicinal products.
You can use the PRE service to view recordings of pre-recorded evidence before trial.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Notices of publication and a consolidated list of references of pre-Exit European Assessment Documents for construction products.
Guidance for businesses on the marking of measuring container bottles, with lists of approved and inactive manufacturers’ marks.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to set up a compost or biogas site, UK and EU standards explained, and alternative treatment methods for animal by-products (ABPs).
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