Case Study
Digitizing Medical Device Field Corrective Actions with IQVIA MedTech
When a manufacturer needed a comprehensive communication and data collection strategy, IQVIA MedTech proved to be a valuable, trusted partner
Jul 20, 2026
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Learn how IQVIA MedTech helped a global imaging company with a large Class II voluntary field action. With over a decade of experience managing and operating recalls and field corrective actions of all sizes, IQVIA MedTech has developed a validated and robust communications process that's compliant with Title 21 of the Code of Federal Regulations (CFR) for electronic records and electronic signatures. The program offers a centralized data repository that tracks, manages, and measures all activities executed on behalf of the manufacturer.
Don’t wait for a recall crisis - be prepared.
IQVIA MedTech’s customized approach executes recalls and field actions quickly and accurately without overburdening your teams. Explore the IQVIA MedTech Recall and Field Action Program.
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Team reviews analytics and market strategies for biotech asset success and patient outcomes in IQVIA biopharma meeting.

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