Proventa International’s Regulatory Affairs Strategy Meeting Europe creates an interactive forum where pre-qualified decision makers from top and emerging biotech, pharma, IT and academic organizations network, share ideas and best practices and discuss pharmaceutical regulation updates.
Amplexor team of subject matter experts will provide guidance and strategic approaches on business intelligence solutions, including RIM and data management during our roundtable discussion. Learn how to take control of your data 11:00-12:00. We’ll see you there!
RIM AND DATA MANAGEMENT ROUNDTABLE DISCUSSION
📅 16 October ⌚ 11:00-12:00
Regulatory affairs experts from around the globe (that includes #AmplexorLSc!) join to share insights and the latest trends revolving regulatory compliance in life sciences industries. In this roundtable discussion hosted by Amplexor team of life science experts, we’ll provide comprehensive approaches for attendees to take their RIM and business intelligence solutions to the next level.
Who should attend?
The event is designed for business leaders from Global Heads to Chief Executive Officers and everything in between, who are responsible for:
- Regulatory Affairs and Operations
- Quality Assurance and Compliance
- Clinical Research and Development
- Data Management
- Document and eRecords Management
- Clinical Operations
- Regulatory Standards Implementation
- Global Submission/Project Management
Why attend?
Whether you’re looking to gain an edge in strategizing your short and long-term goals via Proventa's pre-scheduled one-to-one meetings, or looking to connect with the right professional from Proventa’s vast network of pharmaceutical regulation experts, this is a “must attend event” for anyone in the industry!
Location
Radisson Blu Zurich Airport
Rondellstrasse, 8058 Zürich, Switzerland
More information and registration
Check out what to expect, see the facilitators or request the agenda.
Want to talk RIM with an expert?
Contact us!