From stories to evidence: Quantitative patient-preference information to inform product-development and regulatory reviews
February 15, 2018
Panel: FDA Case for Quality Update
February 6, 2018
Patient Centered Benefit-Risk Assessment
January 22, 2015
Framework for Surrogate Sample Use in Clinical Diagnostic Test Development and Product Submission – from the MDIC Clinical Diagnostics Surrogate Samples Working Group
December 12, 2017
A Case Study in How Patient Preference Information Contributes to Regulatory Decisions for Medical Devices
December 4, 2017
Patient values and P-Values: Exploring a new method for developing patient-centered clinical trials
November 17, 2017
MD&M Minneapolis Event
November 8, 2017
Use of Real-World Evidence to Support Regulatory Decision-Making for Medical Devices
October 10, 2017
AdvaMed 2015
October 5-7, 2015
Grand Rounds: Improving Evidence Generation for Medical Devices: The New National Evaluation System for Health Technology (NEST) Webinar
September 22, 2017
NextGeneration Dx Summit
August 17, 2017
2017 MedTech + Digital Health Summit
July 12, 2017
Transcatheter Valve Therapies (TVT) Conference
June 16, 2017
Virtual Patient R Code Access and Use
May 18, 2017
How Innovation and Cybersecurity Impacts Physicians and the Patients We Treat. Balancing the Risks & Patient Benefits with Medical Technology Advancements
May 11, 2017