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Regulatory Sessions from Veeva's Medical Device & Diagnostics Summit Online

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GE Healthcare: Measuring RIM Results
GE Healthcare shares best practices for measuring success with RIM, including affiliate activity, health authority approvals, and submission rejections.

Baxter: A Model for Successful Regulatory Implementation
A successful RIM implementation requires significant planning, stakeholder involvement, and well-defined processes. In this session, Baxter shares its approach and lessons learned as they prepare and execute their RIM implementation.

Alcon: Planning for EU MDR
Alcon shares their approach as they prepare for EU MDR and best practices for leveraging RIM to meet new regulations while driving efficiency and speed.

Roche Diagnostics: Managing Global Submissions for Greater Speed and Compliance
Learn how to manage the global regulatory submission process to improve collaboration, speed approvals, and reduce administrative burden.

Medtronic: Best Practice in Aligning Business and MLR Review
Medtronic shares best practices for creating a more efficient medical, legal, and regulatory (MLR) review and approval process with focus on change management and measuring success.

Roche Diagnostics: Best Practices for Delivering Compliant Commercial Content
Roche Diagnostics shares best practices for implementing and utilizing DAM to better manage and deliver compliant content.

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