Date: Thursday, May 22, 2018 | Time: 11am EDT / 8am PDT
Cumbersome. Laborious. Error-prone. Wasteful. Fragmented. Painful. There are many words to describe the current state of how many firms engage in over burdensome validation efforts. For those firms still approaching CSV in this manner, there is another way.
Join us for this webinar to learn how to automate and centralize your CSV process into a single data repository. Seamlessly link requirements, feature based risk assessments, and corresponding assurance evidence. It is easy to use and offers dashboards and reports to help your firm easily prepare for regulatory reviews.
In this webinar, which includes a short introductory of Non-Product Computer Systems Validation (CSV) methodology solution demonstration, expert speakers will discuss how these technologies will enable medical device companies to:
Larry Sampson., Industry Specialist - Medical Devices, Siemens PLM
Javier Cubero, Systems Engineer, Medical Devices, Siemens PLM