Webinar: Sailing the RIM High Seas: Navigating through Change
Sponsored by: Veeva Systems
- R I M
Date: 13 December
Days to go: 25
Time: 3PM CET/2PM GMT
Solve Your RIM Challenges with a Unified Approach
Many pharmaceutical companies realize they need to get their data in order to comply with health authority standards. Driving change means rethinking regulatory processes and streamlining siloed systems.
Yet rather than viewing change as a burden, organizations have the opportunity to reframe RIM requirement. Many in the pharma industry are now looking at regulatory transformation as the way forward. In fact, 86% of pharmaceutical organizations are embarking on transformational change, according to a Gens and Associates.
The question is how do you get started?
In this webinar, we will describe the opportunities with regulatory transformation to improve data quality, harmonize processes, and increase efficiency and productivity of your regulatory teams. We will share best practices based on experiences from other companies who have already embarked on their transformation journey. And we will explain how Veeva Vault RIM Suite provides a unified approach to your RIM needs.
Join Veeva and NNIT for this joint webinar on 13 December at 3 p.m. CET. Reserve your spot now!
Sr. Director, Vault RIM, Enterprise - Veeva Systems
Paul leads Veeva’s strategy team for the Vault product in the areas of regulatory and quality. A technologist and business development professional, he has spent the past 23 years in the life sciences industry, following eight years as a software engineer.
Previous roles have included leading the product management function in CSC’s Life Sciences Software Solutions Group. Prior to this, for 14 years he focused on product development, product support, professional services and business development associated with CSC’s Life Sciences solutions, heading up the European Life Sciences organisation during its transition from FCG Inc. into CSC.
Managing Consultant and Line Manager - NNIT
Rune Bergendorff is working within the Regulatory Affairs domain and has vast experience from different projects within RIM, xEVMPD, ISO IDMP and labelling. He is a member of the ISO TC215 WG6 and participates in the EMA SPOR Taskforce. His experience draws on projects from a large number of top 20 pharmaceutical companies acting as trusted advisor.
Key Learning Objectives
- Key drivers for RIM digital transformation
- What the journey looks like and the benefits of such a transformation
- How some organizations have already embarked on their transformation with unified RIM
- Regulatory Affairs
- Regulatory Specialist
- Regulatory Strategy
- Regulatory Intelligence
- Regulatory Operations
- Regulatory Compliance