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In the highly regulated Life Science Industry, compliance with regulations is critical. Learn how to implement and validate a field service platform (or solution) and maintain compliance with regulations, such as the UDI Rule, 21 CFR Part 11, QSR and other medical agency regulation.

The discussion will include:
  • Why do medical device companies need to validate field service platforms
  • What are the FDA and UDI final rule compliance requirements?
  • How companies are achieving improved business process and compliance in the cloud using ServiceMax
  • How USDM Life Sciences and ServiceMax established a better approach to validate ServiceMax
  • Live Q & A session
About the Presenters:

Bryan Coddington

Bryan is an IT professional with in-depth knowledge of cloud, process optimization, integration, and mobile applications for the Life Sciences industry. A Digital Transformation (Dx) thought leader helping companies maximize their investment in cloud-based applications while remaining compliant with GDPR and federal regulations such as 21CFR Part 11, 803, and 820.

Ken Remington

Sr. Director, Sales Enablement, ServiceMax Ken Remington is a Sales and Marketing leader and productive team builder with 20+ years in delivering products to market, enterprise software sales, and business consulting services. Ken has helped drive success for start-ups as well as mid-sized corporations by using his keen sense to identify early market trends.

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