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.