When organizations are leveraging a RIMS (Regulatory Information Management System) solution, affiliates and HQ users might not be following an optimal and harmonized process. Regulatory affairs organizations in the healthcare and life sciences field must shift towards smarter and more intelligent processes for a variety of reasons. Proper RIMS solution selection and implementation can reduce costs, improve efficiency, and reduce timelines for submissions. Moving forward, maintaining the data quality of your solution can help your team prepare for ever-changing national regulations, data requirements, and mitigate uncertainty surrounding regulatory submissions.
Your Regulatory Affairs team needs a solidified plan of action for selecting the right RIMS solution and addressing the expanded regulations. Join us to hear from the perspective of our Regulatory Information Management subject matter expert, Jonathan Sanford.
Celegence will be hosting the WEBINAR on February 24th at 10am EST. Register online now here!