Presented by: Jeff Ramos, Solutions Engineer, ValGenesisChange is the only permanent thing in this world. However, in Life Sciences, adapting to new norms may be slow and can lead to apprehension. Join us in this webinar to learn how you can mitigate those fears and take a path forward to adapt CSA in your workplace.Benefits:Gain […]
Presented by: Rosalind Beasley, CEO and Co-founder, Main and Mission, Inc.Tim Kirkelie, Med Tech Executive / consultant, Main and Mission, Inc.Discover how AI technologies are reshaping the future of compliance, quality control, and data management processes. Gain valuable insights from industry experts and learn how to leverage AI to navigate challenges and drive innovation in […]
Presented by: Dave DeLuca, Lakshmi Chitrapu, and Ken ShitamotoThis webinar covers the following topics:Recognizing the interconnectedness of GxP and non-GxP regulations is key to developing a comprehensive compliance strategy. Integration allows organizations to streamline processes, reduce redundancies, and ensure consistency across regulatory requirements. Achieving synergy between GxP and non-GxP regulations enhances operational efficiency, mitigates risks, […]
Presented by: Philip Jarvis, Director C&Q and Digital Validation Strategy, VEQTORHow digital validation tools are enabling validation 4.0Risk based data integrity processes (importance of data mapping and criticality of data) Building in Data integrity by design into digital validation systems Data integrity guidance watchouts – Bring paper into the digital world compliantly and defining “true […]
Presented by: Dr. José C. Menezes, CSO, ValGenesisJoin us for a webinar where we’ll delve into the practical application of ICH Q12 principles for biopharma operations. Biotech processes prior to QbD use control strategies that lack understanding of criticality and definition of CPPs or CQAs. Discover how to define these parameters from manufacturing history, and […]
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