Resource Download Survey
Please answer the questions below to share with MDIC how you've used a resource from its electronic resource library.
Please indicate which Resource you have downloaded
2017 MDIC EFS Metrics Report: Administration and Clinical Practices
Background Information on Early Feasibility Studies
Case for Quality: CAPA Process Improvement
Case Study: Using the MDIC Patient-Centered Benefit-Risk Framework to support an expanded indication
Clinical Diagnostics Somatic Reference Samples Request for Information
Clinical Diagnostics Somatic Reference Samples Request for Proposals
Cybersecurity in the Medical Device Sector: Coordinated Vulnerability Reporting
Early Feasibility Study (EFS) Contracting Resource: Negotiating Range Process and language Libraries
EFS Participant Landscape
EFS Patient Informed Consent Form Template
EFS/FIH Perspectives Report
Framework for Developing Clinical Evidence for Regulatory and Coverage Assessments in In Vitro Diagnostics (IVDs)
Incorporating Patient Perspectives in Clinical Trial Design and Research
Literature Review: Patient Engagement in Clinical Trials
Maturity Model Report
MDIC EFS Blueprint
MDIC PCOR Project: From P-Values to Patient Values in Parkinson's Disease Workshop Summary
Medical Device Cybersecurity Report
Medical Device Quality Metrics White Paper
Medical Device Quality Outcomes Analytics Report
Patient Centered Benefit-Risk (PCRB) Framework
Patient Centered Outcomes Research Project Overview
Patient Engagement in Clinical Trials Survey Report
Patient Introduction to Consent for Early Feasibility Studies
Press Release: Patient Preference Collaboration
Somatic Reference Sample Project Proposal
SRS Landscape Analysis Report
Surrogate Sample Framework
Surrogate Sample Use Survey Results
TVT 2017 EFS Presentation
What was your primary reason for downloading / using this resource?
Have you found this resource or any MDIC resource helpful as it relates to getting devices to markets? (If yes, please explain)
Any additional information you'd like to share?
MDIC is exploring offering trainings or workshops on resources, would this be something you're interested in?
Would you be willing to be contacted by MDIC or FDA to further discuss your response?
Company / Organization
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