Presented by Jeremiah Quirke
Understand how this world biotechnology leader with over 45,000 employees and facilities worldwide, globally transformed the productivity of its Commissioning and Qualification processes, using Kneat Gx e-validation software’s automated traceability.
Presented by No Deviation
Pharmaceutical Manufacturers are required to demonstrate facilities, systems, utilities, and equipment are suitable for the intended purpose. The ISPE Baseline Guide 5 (Second Edition) provides ‘best of the best’ practical guidance on the implementation of a science and risk-based approach for Commissioning and Qualification (C&Q). Watch this webinar to understand the key principles of ISPE Baseline Guide 5 and how to apply them in a paperless validation environment while exploring the key features and functionality of Kneat.
Discover how Kneat Academy’s professional training programs can help you to increase your productivity, confidence, and competence in Kneat Gx with this webinar presented by Rick Mineo, Kneat Academy Director and Director of Strategic Partnerships.
Building the Future of Validation Together Join Rick Mineo, Director Strategic Partnerships, Kneat, Aaron Roth, Associate Director Global C&Q, CAI,…
How to Budget for Digital Validation & Maximize ROI Join Derek Hughes, VP US Sales, Kneat, Justin Blackwelder, Project Services…
Achieving Computer Software Assurance (CSA) with Digital Validation The FDA recently released its Draft Guidance for Computer Software Assurance (CSA)…
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