August 8, 2019 By Halle Kirsh Webinar: 6 essential strategies for your MDR survival guide – A clinical research point of view
December 4, 2018 By Chris Newmarker Predicting an FDA inspection: Here’s how the CISST algorithm works
August 22, 2018 By Halle Kirsh Webinar: The challenges of inspecting in a complex clinical environment and FDA form 483 consequences
February 20, 2018 By Lisa Rosen Webinar: How to make sense of safety oversight in clinical research — DSMBs, CECs and Medical Monitors
May 23, 2016 By Medical Design and Outsourcing Five hurdles to overcome when planning a medical device trial