Wednesday, June 24th; 11 AM EST | 4PM GMT | 5PM CET
Webinar panelists:
The majority of GxP regulated laboratories, from pharmaceutical R&D units to contract research organisations and medical device manufacturers, still manage their critical records on paper. Binders, printed protocols, handwritten signatures and physical audit trails remain the norm, a legacy of decades in which paper was the regulatory gold standard.
That standard is shifting. Regulators increasingly expect the level of data integrity, traceability and access control that only validated digital systems can reliably deliver, and labs that postpone the transition are not avoiding risk, they are accumulating it. Yet in environments governed by GxP compliance demands, going digital is never a convenience upgrade. It is a validated change that must be planned, documented and executed with the same rigour as any other quality critical process.
This webinar is a knowledge session, not a product demo. It is an honest look at what GxP compliance demands in a digital context, where the complexity truly lies, and how purpose built, validated lab software makes the transition both achievable and defensible.
This session is designed for anyone involved in moving a regulated lab away from paper.
Matjaž Hren is the Vice President of Product Management for SciNote. He started as a researcher with a PhD in Biotechnology (University of Ljubljana), working on projects in both basic and applied science. His career eventually took a turn towards entrepreneurship by co-founding BioSistemika, a life sciences software development company, where he developed SciNote Electronic Lab Notebook, which was later spun out as an independent company. Now, Matjaz leads the Product Development team, advancing SciNote as a digitalization solution for the lab of the future.
Arun brings a wealth of experience from the medical device product development industry, with a strong background in navigating highly regulated environments and adhering to strict quality and regulatory standards. His expertise spans NGS-based and immunoassay-based IVD development, FDA-regulated diagnostics, and systems engineering. At SciNote, Arun works with the company’s largest clients to design custom digital solutions tailored to their needs. His interests in SaaS for biotech, global health, and emerging markets further enhance his ability to deliver impactful solutions in diverse settings.
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