Resource Center - RIM & IDMP

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

November 11, 2021

eCTD, RIM/IDMP

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

October 26, 2021

RIM/IDMP

PhlexRIM's Business Process Automation Explained

RIM/IDMP

Best Practices for RIM Business Process Automation

October 15, 2021

RIM/IDMP

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

September 3, 2021

Automation, RIM/IDMP

PhlexRIM End-to-end Regulatory Information Management System Overview

RIM/IDMP

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

August 25, 2021

Automation, RIM/IDMP

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

July 23, 2021

Automation, RIM/IDMP

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

RIM/IDMP

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

July 14, 2021

Automation, RIM/IDMP

IDMP Readiness: Updates and Best Practices

May 5, 2021

RIM/IDMP

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

April 7, 2021

RIM/IDMP

10 Key Steps to Help you Prepare for IDMP Compliance

February 24, 2021

RIM / IDMP, Outsourcing

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

January 20, 2021

eCTD; TMF; RIM/IDMP

Industry Survey Results & Expert Analysis

October 29, 2020

eCTD; TMF; RIM/IDMP, Automation

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

October 29, 2020

eCTD; TMF; RIM/IDMP, Automation

Innovations In IDMP Preparation: Perspectives from Sponsors

September 8, 2020

RIM/IDMP

The Journey from File to Trial: Automating Regulatory to TMF

August 26, 2020

Automation, TMF, RIM/IDMP

Validating an AI Solution with a Focus on Clinical and Regulatory

August 12, 2020

Automation, TMF; RIM/IDMP

Trial to File to Trial + Archiving: Innovative Approaches to meeting Archiving Requirements

July 22, 2020

TMF; RIM/IDMP; Outsourcing

Innovation on IDMP / Data Preparation

July 15, 2020

RIM/IDMP

Phlexglobal Providing Vital Support for COVID-19 Clinical Trials

June 2, 2020

TMF; Outsourcing; RIM/IDMP

New Insights into COVID-19 Drug Development

May 5, 2020

TMF; RIM/IDMP

Updated FDA Guidance on Clinical Trial Conduct During COVID-19

May 5, 2020

TMF; RIM/IDMP

Regulatory Robotic Process Automation: The Evolution from Compliance Enablement to Compliance Automation

May 4, 2020

Automation;  RIM/IDMP

Leveraging Automation for IDMP Readiness

April 29, 2020

Automation, RIM/IDMP

AI Powered Automation Proven in Life Sciences

April 20, 2020

Automation; TMF, RIM/IDMP; IDMP

New Developments in IDMP: What You Need to Know, and What You Can Do Today

April 9, 2020

RIM/IDMP

Solutions to COVID-19 Business Continuity and Fast Track Trial Challenges – Clinical and Regulatory Aspects

April 1, 2020

TMF; Outsourcing; RIM/IDMP

How Automation is Transforming Regulatory Compliance in Life Sciences

March 25, 2020

Automation, RIM/IDMP

Prepare yourself for 2020 – Global regulatory update

December 6, 2019

eCTD, RIM/IDMP

FDA at DIA RSIDM 2019 – Presentations Highlights

February 18, 2019

IDMP/RIM

SPOR Update 2018 – News from the EMA webinar

March 15, 2018

RIM/IDMP

The Challenge with EMA’s Changing Timelines for IDMP

July 18, 2017

RIM/IDMP

Regulatory Information Management – traditional vs. modern

June 15, 2015

IDMP/RIM