The Medicines and Healthcare products Regulatory Agency (MHRA) is launching a new publication – the Good Clinical Practice Guide – which covers legislation, guidance and good practice relating to the conduct of clinical trials of medicinal products for human use in the UK.
The guide includes commercial and noncommercial sponsors and hosts of clinical trials, as well as contract research organisations, clinical research consultants and other niche providers. It also references European legislation and guidance as well as international standards.
