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 RIM Resource Center




JOURNAL ARTICLE: Industry and Regulators Push Ahead to a Digital 2023

February 22, 2023

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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Entering the Post-Paper Realism: The Principles of Cyber Ethics

The Shoulds and Shouldn’ts of Electronic Systems and Data in Clinical Trials Intro With the word should being mentioned 569 times and constituting ~7% of the content (only outweighed by data – 618

Overcoming TMF misfiles and metadata errors to reduce inspection risk

Trial master file misfiles are a common occurrence, with as many as one in every 10 documents being misfiled.   In some ways, misfiles are an even greater issue now with eTMF systems, where filing is

TMF Management in Clinical Trials Blog 3: Running the Trial in Your eTMF

Introduction Well, first and foremost, welcome!   Rob Jones has relinquished control and I’ve been given free rein to bring you the last blog in the series on TMF Management in Clinical Trials. Those

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