Subject: Starting a RIM project? Make sure you don’t miss the big picture.

Regulatory Webinar

Benefits of Implementing an

End-to-end RIM Platform

Thursday, December 8, 2022

11:00 AM – 11:30 AM EST

5:00 PM – 5:30 PM CET


Why should you consider a Regulatory Platform instead of a standalone RIM solution? In less than 30 minutes, learn first steps, realistic objectives, and business benefits when implementing an end-to-end RIM.


In this presentation we will explore the benefits of a state-of-the-art end-to-end regulatory information management platform. We will see what is desirable and what is practical in 2022.


  • Understand the capabilities of a RIM platform

  • Learn good practices for implementing processes

  • Discover how to confront common challenges

  • Outline initial objectives for your RIM project

  • Discover proven benefits via Use Cases

Speaker

Steve Clark

Regulatory expert

Email: sclark@ennov.com

Visit us: https://www.ennov.com

Steve has a Master’s Degree in Immunology from the University of Essex, UK and over 25 years of experience serving in various senior Regulatory Affairs and Regulatory Operations roles for companies including Gilead, Amgen, Merck, Baxter and Parexel. He is responsible for the implementation of Ennov Regulatory systems and assisting the development of the Ennov Regulatory product suite.


 

Ennov develops innovative, powerful and easy-to-use software for document and process management. Ennov has specialized its software to meet the specific needs of the health and life sciences sectors: Quality, Pharmacovigilance, Clinical Studies and Regulatory Affairs.