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 RIM Resource Center




WEBINAR: The Next Phase of Intelligent Regulatory Business Process Automation is Here

April 20, 2022

PRESS RELEASE: Cary Smithson Brings Extensive Life Sciences Regulatory Expertise to Help Phlexglobal Customers Navigate a Transforming Regulatory Landscape

November 11, 2021

PRESS RELEASE: Phlexglobal Announces Industry’s First RIM Software with Intelligent Business Process Automation

October 26, 2021

VIDEO PhlexRIM's Business Process Automation Explained


WHITE PAPER: Best Practices for RIM Business Process Automation

October 15, 2021

CASE STUDY: How a Top 5 Pharmaceutical Company Improved Compliance Speed and Consistency with RIM Business Process Automation

September 3, 2021

VIDEO: PhlexRIM End-to-end Regulatory Information Management System Overview


WEBINAR: PhlexRIM 2.0: The First Regulatory Platform with Built-in Process Automation

August 25, 2021

CASE STUDY: How a Top 20 Pharmaceutical Company Leveraged Artificial Intelligence to Prepare for IDMP

July 23, 2021

DATA SHEET: PhlexRIM dramatically improves compliance with efficient and effective real-time access to your global registration information


WEBINAR: The Bridge Between Clinical & Regulatory: How CTR and CTIS are Revealing the Need for more Holistic Approaches

July 14, 2021

WEBINAR: IDMP Readiness: Updates and Best Practices

May 5, 2021

WEBINAR: When RIM is not Enough: Overcoming the Limitations of Document-Driven Systems

April 7, 2021

WHITE PAPER: 10 Key Steps to Help you Prepare for IDMP Compliance

February 24, 2021

WEBINAR: From File to Trial to File: Benefits of an Integrated Clinical and Regulatory Perspective

January 20, 2021

WHITE PAPER: Industry Survey Results & Expert Analysis

October 29, 2020

WEBINAR: Innovation Tour Survey Results Panel: Future Trends in TMF, IDMP, and eCTD

October 29, 2020

ARTICLE: Innovations In IDMP Preparation: Perspectives from Sponsors

September 8, 2020

WEBINAR: The Journey from File to Trial: Automating Regulatory to TMF

August 26, 2020
WEBINAR: Validating an AI Solution with a Focus on Clinical and Regulatory August 12, 2020




















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Clinical Trials & the TMF 101 - Blog 4: The TMF Trinity

Introduction We have been on a journey you and me, we started off by understanding the purpose of a clinical trial and the multiple phases to get products to market. We then looked at the Trial

Clinical Trials & the TMF 101 - Blog 3: Paper vs Electronic, why it is more than a DMS

Introduction Awww it warms my heart you came back to read the third blog. I hope you are finding these helpful, don’t forget to send any of your feedback or questions to We

Clinical Trials & the TMF 101 - Blog 2: What is this TMF you speak of?

Introduction You came back, great! I hope you enjoyed our first blog in this series which was all about the basics of a clinical trial. In this blog we are going to get into the Trial Master File,

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