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What Needs to Be in Place Before a First-in-Human Trial Begins Before entering a First-in-Human trial, a drug candidate must be supported by a comprehensive package of scientific, non-clinical and quality evidence

Patients should not assume that MHRA approval automatically translates to immediate NHS availability in any part of the UK

The product is supplied in capsule form for laboratory research purposes

FDA and Novo Nordisk are testing the seized products and do not yet have information about the identity, quality or safety of these drugs

The other author has no conflict of interests related to this publication