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20th - 22nd April 2021
★ 100% virtual conference ★Presented in Central European Time (CET)

The IDMP deadline is looming. Did you use your time wisely?

Elevate Your RIM System From Disorderly Documents To Dependable Data With Direct Advice From 8 IDMP Taskforce Members, Regulatory Authorities, and Industry Pioneers

The digital age of regulation is here. Time-critical insights to stay Ahead.

RIM: The Key to Regulatory Compliance

  • Do you have a harmonised RIM system? Get one with case studies from Alexion and Novartis
  • Can your RIM system accelerate your submission? It should do. Learn how with Roche
  • What does the future of RIM look like? Hear from Taskforce Members Argha Nag and Rodrigo Palacios 

Regulatory Success: It’s All About Data

  • Get clean data and keep it that way! Ensure you have one single version of the truth with case studies on data cleaning and maintenance  
  • Who owns your data? Hear a case study on Data Governance  
  • Learn how to align your data system with a case study from Novartis 

IDMP Focus Day: Get 2022 Ready

  • Take home the latest requirements and timelines with IDMP Taskforce leadeLaurent Desqueper, Merck and National Competent Authority representative Ana López De La Rica Manjavacas, AEMP 
  • Be prepared to migrate your data from XEVMPD to IDMP with Associate Director, Data Stewardship & Compliance, Bristol-Myers Suibb   
  • Hear case studies with leading Pharma companies on how they’ve got IDMP ready, including: GlaxoSmithKline, Johnson & Johnson, Takeda and more   

Now is the time to take action. What answers do you need?

Connect you with pharmaceutical regulatory pioneers to help you: 

Move Away From Paper into the Digital Age of Regulation

Achieve Regulatory Compliance with your RIM System

Pave the Way for More Cohesive Business Operations

Uncover the Secrets to Organised and Clean Data

Maintain IDMP Compliance

Prepare for the Future of Regulations