Associate Manager, Medical Device Services Celegence
Description: Join us for an enlightening session that uncovers the depth of our expertise in Clinical Evaluation and Post-Market Clinical Follow-up (PMCF) Strategies. Discover the pivotal role of cutting-edge tools and how they can synergize to introduce unparalleled efficiency into your regulatory practices. From navigating common notified body observations to optimizing data presentation, this session offers a strategic blueprint for achieving clinical evaluation excellence by leveraging the transformative power of AI and technology for regulatory compliance.
Learning Objectives:
Understand the promising potential of AI in crafting robust Clinical Evaluation and PMCF Strategies.
Explore real-world examples of AI-driven approaches to enhance compliance and streamline regulatory processes.
Identify common notified body observations and develop strategies to proactively address and prevent them.
Learn best practices in utilizing technology to optimize data presentation for Literature and PMCF pathways.
