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PLM & Requirements Management (RM) in Ensuring Compliance across the Lifecycle

Presented by Laurence Sampson

As is the case in most industries these days, there is a heavy regulatory component within medical device manufacturing. Effective regulatory change management and compliant response across a multiple-team operated company is challenging and requires heightened transparency and collaboration. Laurence (Larry) Sampson joins PI to discuss the two-part deployment of PLM and RM in remaining consistently compliant.

  • Deploying PLM to tackle challenges in engineering change orders, compliance and quality management
  • Why cloud PLM?
  • Integrating PLM with existing enterprise tools
  • Integrating other processes into PLM including CAPA, Quality and Post-market ops
  • Deploying RM to offer flexibility in business software development
  • Authoring, linking and tracking requirements effectively
  • Extracting ideas from PLM's documents
  • Why not integrate PLM and RM?
  • What has RM meant for traceability and collaboration across the lifecycle?
Laurence Sampson, Siemens PLM
Laurence Sampson

Sr Director Medical & Lifescience Industry Strategy, Siemens PLM

Laurence Sampson is an accomplished technical manager with over 20 years of medical device experience including high volume process and product development projects.  Laurence is currently Senior Director Medical & Lifescience Industry Strategy, and holds a B.S. in Mechanical Engineering from Colorado State University, and a M.B.A. from the University of Denver.