Mastering Compliance: Essential Insights into PMS Documentation - Webinar
Автор: Celegence
Загружено: 2025-11-23
Просмотров: 14
Gain invaluable insights into ensuring compliance with regulatory requirements and learn best practices to enhance your organization’s PMS documentation processes. Whether you’re a regulatory affairs specialist, quality assurance professional, or involved in product development, this webinar is tailored to equip you with the necessary knowledge to stay ahead in the ever-evolving landscape of medical device compliance.
Webinar Speakers:
Dr. Anushree Singh, Manager, Medical Device Services
Kasturi Rao, Team Lead, Medical Device Services
Unlock actionable insights with our webinar focusing on key learning objectives:
1. Understand the Essential PMS Components
2. Master Effective Data Collection Strategies
3. Leverage Technology for Enhanced Precision and Productivity
4. Strategize PMCF Pathway
5. Navigate Observations from Notified Body
Celegence – Regulatory Services and Solutions to Support the Medical Devices and Diagnostic Industry
Celegence offers regulatory solutions and services that are tailored to the needs of medical devices and In Vitro Diagnostics (IVD) manufacturers. The benefits of our solutions and services include clear visibility and control over diverse product portfolios, increased operational efficiency, lowered costs, and ongoing regulatory compliance.
For further regulatory assistance or queries on how Celegence can support your organization, reach out to [email protected] today.
Доступные форматы для скачивания:
Скачать видео mp4
-
Информация по загрузке:
