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Quality and the handling of quality issues are huge concerns for any life sciences company. In order to avoid fines and potentially the ability to market a product, companies must adhere to the rigorous compliance requirements of the FDA. Let USDM Life Sciences and 123Compliance, the maker of cloud-based compliance solutions, show you how to automate your Quality Management processes and procedures.

  • Customer facing vs. internal processes
  • Ownership of customer communications
  • Complaints and adverse events
  • Customer self-service
  • Live Q & A session

About the Presenters:

David Blewitt
David Blewitt

Vice President of Cloud Compliance David is an accomplished life sciences regulatory and IS compliance professional with more than 25 years of experience in the pharma, medical device, biotech, and blood management industries, specifically in the fields of computer systems validation, risk management, quality assurance, software development, product life cycle management, and compliance roadmap development.

Plarent Ymeri
Plarent Ymeri

CEO, 123Compliance With more than 14 years of experience in the life science and healthcare industries, Plarent brings direct knowledge and expertise of software organization leadership, development, implementation and validation.

Bryan Coddington
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.

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