NEST is updating its Research Methods and Data Quality Frameworks to improve the rigor and reliability of real-world evidence (RWE) in medical device evaluation, and is seeking public feedback to ensure these frameworks remain valuable for regulatory and clinical decision-making.
Author: Matthew Victoria
MDIC Releases Final Pilot Report on MedAccred® Sterilization Program
The Final Pilot Report provides recommendations for FDA’s consideration regarding the potential use of MedAccred audit data in risk-based inspection planning and resource allocation.
MDIC In the News: How Benchmarking Data can Improve Medical Device Security
MDIC’s Jithesh Veetil and Medtronic’s Chris Reed discuss how benchmarking data helps medical device manufacturers assess security maturity, justify investments, and strengthen cybersecurity practices.
MDIC In the News: Harness MDIC’s Resources to Strengthen Clinical Trials and Patient Outcomes
Joseph Sapiente, MDIC’s chief science and technology officer, shares how collaboration across stakeholders helps strengthen clinical trials, enhance genomic testing, and integrate real-world evidence to improve patient outcomes.
MDIC In the News: What’s Trending In Medical Devices And Diagnostics For 2025?
Drawing from their extensive expertise, four program directors from MDIC share their predictions on the trends that will drive innovation and reshape clinical research in 2025.
Accelerating the Adoption of Advanced Manufacturing Technologies to Improve Quality, Access, and Outcomes
Advanced Manufacturing is transforming the medical device industry with technologies like 3D printing, AI, and robotics. Explore key findings from an MDIC study on barriers and opportunities driving advanced manufacturing adoption in 2024.
MDIC In the News: MDIC Backs Dr. Tarver as New CDRH Director
MDIC President and CEO Andrew C. Fish provided insights for the MedTech Dive article announcing her appointment, highlighting her visionary leadership and the shared commitment to improving patient outcomes.
MDIC In the News: Andy Fish Welcomes Dr. Michelle Tarver as the New Director at FDA’s CDRH
In an article by MD+DI, MDIC expressed strong support for Dr. Tarver’s appointment, recognizing her visionary leadership and dedication to improving patient care.
MDIC In the News: NEST’s Simon Mason Discusses Real World Evidence Studies
In this insightful episode of the Global Medical Device Podcast, host Etienne Nichols is joined by Simon Mason, President of NEST (National Evaluation System for Health Technology), to explore how real-world evidence (RWE) is shaping the future of medical device regulation.
Participate in the 2024 MDIC Medical Device Cybersecurity Benchmarking Assessment
The MDIC Maturity Cybersecurity Benchmarking Assessment evaluates cybersecurity maturity across the medical device sector. Developed in collaboration with the Health Sector Coordinating Council (HSCC) and Apraciti, this comprehensive tool seeks to establish a standardized measure of cybersecurity practices, identify areas for improvement across the industry, and drive advancements in cybersecurity protocols for medical technologies.