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Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Professional conduct panel outcome, including decision and reasons.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
Outlining the principles for the management and oversight of the import of investigational medicinal products (IMPs) to Great Britain from listed countries.
Apply to become or identify an approved manufacturer authorised to carry out conformity assessment.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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