Business & Regulation

We dive into the archive of 2021 for insight and inspiration – this time with Peter Marks

We ask James Chambers from Tufts Medical Center about the challenges faced by biosimilars in the US.

Audrey Greenberg on FDA staffing cuts, Peter Marks’ resignation, CDMO pressure, IP migration, AI acceleration, and what CGT needs now to stay on track

Resignation letter states: “truth and transparency” around vaccines are not desired by Health Secretary RJK Jr.

Rumours claim that a well-known vaccine skeptic has been appointed to lead study on links between vaccines and autism.

An industry survey looks at changing attitudes and challenges in digital innovation for clinical research. Uptake is slow but steady.

Thoughts on the US National Institutes of Health and its role in funding research for non-opioid therapeutics.

FDA letter sent to Edenbridge Pharmaceuticals demonstrates the challenges of getting pharma advertising right.

Neal Baer, editor of a collection of essays on CRISPR, says we must not overlook the dark side of the technology.

The role of digital technologies in optimizing traceability in pharmaceutical supply chains.