Getting MDR Clinical Evaluations Right: Practical Guidance for Dental Device Manufacturers
Overview
Where
Online Webinar
When
10:00 AM ET
Why Your Regulatory Data Processes May Be Costing More Than You Think
Despite growing regulatory demands and advancements in data standards, many pharmaceutical companies still depend on spreadsheets, PDFs, and legacy tools to manage their regulatory operations. These traditional methods often hide inefficiencies, increase compliance risk, and slow down submissions — resulting in what we call data chaos.
Join Celegence on September 2, 2025, for an essential webinar that explores the hidden costs of disjointed data practices in regulatory affairs. Led by John Popp, Regulatory Data Management Manager at Celegence, this session will provide a practical roadmap for teams aiming to build a structured, resilient, and future-ready regulatory data ecosystem.
Who Should Attend?
This session is tailored for regulatory professionals navigating increasing data complexity, including:
- Regulatory Affairs & Operations: Managers, Submissions Leads, Global RA Roles
- RIM & Data Governance: RIM Specialists, Data Stewards, IDMP/MDM Leads
- Regulatory Technology & Systems: IT Business Analysts, Systems Managers
- Quality & Compliance: QA and Regulatory Compliance Professionals
- Labeling & Structured Content: Labeling and Structured Authoring Teams
- Regulatory Strategy & Leadership: VPs, Heads of RA/RO, Regulatory Innovation Leaders
What You Will Learn
Key Takeaways for Regulatory and Data Teams:
- The Hidden Costs of Legacy Tools: Understand how reliance on manual processes introduces inefficiencies, compliance risks, and operational delays.
- Structured Data Submissions – What They Mean for You: Learn how regulatory requirements are evolving and what structured submissions demand from your internal systems.
- Governance & Ownership Best Practices: See how proper data stewardship, clear ownership, and governance models can reduce risk and boost efficiency.
- From Reactive to Proactive: Get strategies to move from patchwork fixes to long-term data quality management.
- Maximizing Value Through Automation & Collaboration: Discover how regulatory teams can unlock greater value through digital tools, structured content, and cross-functional workflows.
Webinar Speakers
Manager – Regulatory Data Management, Celegence
John Popp
John Popp brings deep expertise in xEVMPD, IDMP, RIMS, and global Regulatory Affairs. He has helped numerous pharmaceutical companies transform their regulatory operations—implementing the right systems, extracting and cleansing data, streamlining documentation processes, and enabling high-impact digital change. His insights are grounded in real-world implementation experience and a practical approach to regulatory innovation.
Where
Online Webinar
When
10:00 AM ET
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27 May, 2025
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