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
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
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
IDMP Focus Day: Get 2022 Ready
- Take home the latest requirements and timelines with IDMP Taskforce leader Laurent 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:
