Author: Matthew Victoria
Accelerating Medical Device Trials with Data Harmonization – Audience Q&A
Patient Engagement Estimation Tool: Tackling the Early-Stage Patient Input Challenge
Boston Scientific Joins NEST Governance Committee
Contribute to the Future of RWE: NEST Seeks Feedback on Updated Frameworks
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.
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.