Law stated as at 01 Jun 2023 • USA (National/Federal)
A Q&A guide to life sciences regulation in the United States.
This Q&A provides a high-level overview of key practical issues, including life sciences clinical trials, manufacturing, marketing, abridged procedure, pharmacovigilance, data privacy, packaging and labelling, biological medicines, medical devices, health care IT, combination products, borderlines, and natural health products.