Date :
Place : United States, Baltimore, md
Contact Person:Eevnt Manager
Description:
Understand Verification and Validation, differences and how they work together Develop a "Working Definition" of V&V, Qualification, and related terms Discuss recent regulatory expectations Software Verification & Validation requirements of the FDA and ISO. The latest FDA Software Guidance & Regulations, including Part 11 -impact on V&V strategies Device and Manufacturing software requirements for V & V How to determine & demonstrate an appropriate V & V strategy How to determine & handle software for different Levels of ConcernDeadline for abstracts/proposals : 19th September 2017
Organized By :NetZealous DBA as GlobalCompliancePanel
Keynote Speakers : David R. Dills, Global Regulatory Affairs & Compliance Consultant currently provides regulatory affairs and compliance consultative services for early-stage and established Class I/II/III device, IVD, biopharmaceutical, cosmetics and nutraceutical manufacturers on the global landscape, and has an accomplished record with more than 27 years of experience in the areas of Regulatory Affairs, Compliance and Quality Systems. He has been previously employed, with increasing responsibilities by dev
Conference Highlights :Regulatory Affairs Management Regulatory Affairs Specialist Auditors Compliance Quality Assurance Management Engineering/Technical Services Operations/Manufacturing Consultants Quality Assurance or Quality Control Professionals IT/IS R&D Production Management
Venue :Baltimore, MD, United States
Check the event website for more details.