How to Optimize the ROI on Your RIMS Solution – Webinar

• What: Webinar on how to optimize the ROI on your RIMS solution
• When: February 24^th at 10am (EST)
• Where: Online Event
• How: Register Here
• Why: Join us to understand the best approach to take in selecting the right RIMS solution  and explore potential integrations with other process areas/functions, and hear our thoughts on the operational challenges facing regulatory affairs teams.

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 24^th at 10am EST. Register online now here!

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.

• 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

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

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

How to Optimize the ROI on your RIMS Solution webinar will be held on February 24^th at 10am EST. Make sure you secure your spot at the webinar by registering now.

Webinar Registration Is Open Now!

Join Celegence for a webcast where our Regulatory Information Management subject matter expert, Jonathan Sanford will discuss the best approach to take in selecting the right RIMS solution.

Secure Your Place Now!

As regulatory specialists, we work across all phases of the product lifecycle from regulatory strategy, authoring, and all aspects of established product maintenance. This includes submission management, publishing, and health authority interaction. We leverage a global team of consultants to provide local regulatory insight, strategy, and intelligence support. We are happy to share our insights with you through the webinar and hope that you can join us then.