Safety is always a paramount concern, especially as medical devices, combination products, and in-vitro diagnostics (IVD) become increasingly important in the management and delivery of patient care
Now more than ever, having the proper framework for the collection and reporting of safety data to ensure both patient safety and efficacy during a clinical trial is essential.
On Tuesday, Nov. 17 at 4 pm ET, Clinlogix’ Jen Kratz, director of safety services, and Solange Bishop, clinical data manager, will present the more pressing challenges of recording adverse events.
During this presentation attendees will learn about the challenges and best practices for medical device clinical trial Safety Management, including Severe Adverse Event (SAE) data capture and cleaning to ensure uniform data for regulatory submissions and clinical data analysis.
Go here to register for this DeviceTalks Tuesdays event.
