Poor patient safety, record keeping common violations in clinical trials

Failure to protect patient safety and maintain documentation were among the most common violations US regulators cited in warning letters regarding the conduct of clinical trials, according to new data.“All research stakeholders have a fundamental responsibility to conduct ethical clinical trials following the principles of good clinical practice,” researchers wrote in the Journal of Medical Ethics.

BLOG: Is the FDA finally moving forward on novel IOLs?

For many years now, a forlorn expression has crossed the faces of American doctors when a non-United States speaker approaches the podium to describe IOL designs available only in their countries.Presbyopia-correcting IOL (PC-IOL) technologies available here are beyond 10 years old and, except for Crystalens (Bausch + Lomb), we still don’t have toric PC-IOLs. And what of promising implants like the dual-optic Synchrony IOL?