Blog
March 3, 2023
3 Key Takeaways from DIA’s RSIDM Forum 2023
DIA recently hosted its RSIDM Forum in North Bethesda, MD. Here are a few of our key takeaways from the event.
January 26, 2023
Does Your Clinical Trial Master File (TMF) Have You Wishing for a Time Machine? 3 Quick Tips
When your trial master file (TMF) is a mess, it can leave you wanting to turn back time. Here are three quick tips for success.
January 20, 2023
How to Plan for a New Pharmacovigilance System
Proper planning is essential when it’s time to implement a new pharmacovigilance system for your organization. Here’s how to get started.
November 10, 2022
7 Key Takeaways from Veeva R&D and Quality Summit 2022
Finding the ideal RIM solution for your team can be a challenging endeavor. That’s why we came up with six steps to help you choose.
July 28, 2022
How to Choose the Right RIM Solution for Your Future Needs: 6 Steps
Finding the ideal RIM solution for your team can be a challenging endeavor. That’s why we came up with six steps to help you choose.
June 9, 2022
4 Steps to Modernizing Your Legacy LIMS
Find out how modernizing your LIMS can optimize your business and streamline the way you work with data.
May 19, 2022
Is the Generis CARA Life Sciences Platform the Tool for Your Future Needs?
In this blog, we look at whether the Generis CARA Life Sciences Platform can be the all-in-one solution you need.
April 29, 2022
Plan for a New eTMF System: 2 Phases
When you move to a new electronic trial master file (eTMF) system, leverage industry experience for a smooth process.
March 7, 2022
Is Vault RIM the Tool for Your Future Needs?
In this blog, we look at the Vault regulatory information management system to see whether it can be the solution for your regulatory needs.