How Much Risk Will Patients Accept?

November 15, 2016

MD+DI article explains how MDIC’s new collaborative project to integrate patient preferences into clinical trials may change how clinical trials are designed.

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New Clinical Trial Approach For Urgently Needed Therapies Could Be On Horizon

October 23, 2016

Medtech Insight article on MDIC’s new initiative to move clinical trials from generic p-values to therapy-specific patient values features interviews with our key collaborators. Also check out this blog post on the initative from The Michael J Fox Foundation.

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Vodcast: Project Aims To Give Greater Value To Patient Preference

October 21, 2016

Medtech Insight interviews MDIC CEO Bill Murray at the 2016 AdvaMed conference about MDIC’s new initiative to move clinical trials from generic p-values to therapy-specific patient values. See the video here.

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Medical Device Innovation Consortium (MDIC) announces new collaboration to move clinical trials from generic p-values of 0.05 to therapy-specific patient-values

October 18, 2016

MDIC announces new collaboration to move clinical trials from generic p-values of 0.05 to therapy-specific patient-values. Read announcement here.

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CfQ: Comparative analysis of medical device quality

October 11, 2016

MDIC Case for Quality issues first report on comparative analysis of medical device quality. Read announcement here.

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A team of authors from the MDIC Patient Centered Benefit-Risk Steering Committee had an article about the MDIC Patient Centered Benefit-Risk Framework published online in the journal Value in Health.

October 3, 2016

A team of authors from the MDIC Patient Centered Benefit-Risk Steering Committee had an article about the MDIC Patient Centered Benefit-Risk Framework published online in the journal Value in Health.

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Case for Quality working group on Product Quality Outcomes Analytics

September 26, 2016

Just released! The full report from the Case for Quality working group on Product Quality Outcomes Analytics is now available in the CfQ Resource Center for Sustained Quality. “Feasibility and Effectiveness of Analytics for Medical Device Product Quality Outcomes” summarizes the team’s work, observations and recommendations as they explored the use of medical device quality data to guide provider value analysis committee purchasing decisions toward better outcomes and cost management.

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(NEST) Planning Board released their recommendations for a NEST Coordinating Center

September 19, 2016

The National Evaluation System for health Technology (NEST) Planning Board released their recommendations for a NEST Coordinating Center in its third planning board report. Recommendations included “parameters for operational leadership, bylaws, and the creation of a representative governing board, as well as several demonstration projects meant to build the foundation of NEST and demonstrate how to more efficiently meet the public’s needs.” MDIC is honored to have been named the NEST Coordinating Center. Learn more about the National Evaluation System for health Technology here.

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More Data Is Not Always Better In Device Trials, Experts Say

August 19, 2016

MDIC Clinical Trial Innovation and Reform report on excessive data collection in clinical trials highlighted in the Gray Sheet. Download the MDIC report and view our recent MDICx webinar on Clinical Trial Quality by Design, which highlighted some results from the report.

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