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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 and the TMF 101 - Blog 1: Basics of a Clinical Trial

Introduction  Firstly, welcome, it is great to see you here. Thank you for taking the time to check out our new blog series on the basics of Clinical Trials and the TMF. This series is designed to be

FDA and MHRA Say Remote and Hybrid Inspections to Continue

At the 2022 Drug Information Association Annual Meeting, held in-person in Chicago June 20-23, representatives from the compliance offices of the FDA and MHRA gave a detailed assessment of the pros

Examining the Why and How of Integrating Your eTMF and CTMS

Adapted from a Phlexglobal Ask An Expert interactive discussion held May 11, 2022 and available on-demand here.   Why Integrate Your CTMS and eTMF Systems?  A typical electronic Trial Master File

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