WEBINAR
Adopting a RIM Platform in MedTech: Myths vs. Reality
Thursday, September 26, 2024
1:00 PM - 2:00 PM US Eastern Time
PROGRAM:
Implementing a Regulatory Information Management (RIM) platform can significantly enhance regulatory processes. However, several misconceptions often prevent medical device companies from adopting these platforms. In this webinar, we'll debunk the most common myths and demonstrate how RIM platforms can quickly generate ROI.
LEARNING OBJECTIVES:
- Learn to identify and debunk the most common myths about adopting RIM platforms in the MedTech industry, helping you make informed decisions about integrating RIM solutions.
- Gain insights into how RIM platforms can provide a robust return on investment by enhancing regulatory workflows, integrating smoothly with existing systems, and improving overall regulatory efficiency and compliance.
WHO SHOULD ATTEND:
Regulatory Professionals from MedTech companies - the presentation is designed to inform and enable senior regulatory roles from mid-large medical devices manufacturers.
SPEAKERS:
Soumya Mahapatra, CEO, Essenvia
Dhriti Roy, VP of RA Transformation, Essenvia