Achieve IDMP Compliance with a Unified Regulatory Solution
With mandatory ISO IDMP compliance beginning in 2023, life sciences organizations should start getting their regulatory systems for submission and tracking into shape. This includes locating the data required for submissions, updating your system architecture, and putting the right data governance in place. To help organizations prepare for this transition, NNIT has developed a framework that ensures high data quality while leveraging Veeva’s Vault RIM Suite for reviewing, submitting, and archiving data provided to EMA.
With less than 2 years left until mandatory compliance, it’s more important than ever to fully understand the impact that IDMP will have on your organization. Join this webinar to hear more about how to get data-ready for IDMP compliance and realize the benefits of a unified regulatory solution.
Join this webinar and learn how to get ready for IDMP compliance.
Agenda:
- Getting started – understanding system architecture, data governance and data readiness
- Get ready for PMS submission with Veeva’s IDMP solution for Vault RIM
- Do you know your data? How to ensure the necessary data quality with NNIT’s Data Quality Services
