Taking Advantage of the EU MDR Delay in Uncertain Times – Webinar
Overview
Where
Online
When
10am EST
Webinar Background
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!
Webinar Featured Presenter – Jonathan Sanford
Jonathan Sanford has been working in the field of Regulatory Operations for the past 18 years and has over 30 years pharmaceutical experience. He has managed a team of Regulatory Operation professionals responsible for publishing regulatory dossiers across Europe, Asia and Latin America. He has been the business lead on a number of Global Document Management Systems, Regulatory Publishing Systems, and RIMS implementations.
How Optimize ROI Your RIMS Solution – Webinar Agenda -Celegence
Webinar Agenda: How to Optimize the ROI on Your RIMS Solution
Discussion of the greatest operational challenges facing regulatory affairs team
Explore the potential integrations with other regulatory process areas/functions to help identify and extract the data you need
Practical Examples and Case Studies
Q/A session with our expert panelist
What You Will Learn
Webinar Learning Objectives Upon conclusion of the program, you will be able to:
- Understand the best approach to take in selecting the right RIMS solution considering cost, useability, and migration capabilities
- Learn the best ways to manage and organize your internal teams, the processes and data, and understand what the best regulatory information management strategies and technological approaches are
- Examine the importance of managing the data quality – internal vs external
- Find out what aspects to consider in adopting an accurate RIMS solution globally and addressing expanded regulations
Webinar Speakers
Who Should Attend?
This webinar would support those working for companies in the life sciences, including pharmaceutical companies, with a special emphasis on:
Quality and Regulatory
Engineering and Operations
Quality Assurance
Research & Development
Webinar Sign Up
How to Optimize the ROI on your RIMS Solution webinar will be held on February 24th at 10am EST. Make sure you secure your spot at the webinar by registering now.
Authored By
Celegence Admin
Where
Online
When
10am EST
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25 Apr, 2025
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