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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.

Field Service Compliance for Medical Devices

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.

Bryan Coddington

Ken Remington

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