Missed our live webinar? No worries! You can now register to access the recording at your convenience. Dive into the essential components of a viable sampling program and discuss key elements that an organization should consider when developing its program.
Lessons from the field: digitalizing environmental monitoring with SherpaPharma
Abstract:
What does EM digitalization look like in practice? Join this client-led webinar to explore real-world digital transformation journeys in environmental monitoring. SherpaPharma users from biotech, biopharma and contract labs will share firsthand experiences; from implementation hurdles to operational wins, offering practical insights to help peers in GMP-regulated environments navigate their own digitalization paths.
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Digital transformation in pharmaceutical quality systems can be complex but the right tools and partnerships can make the journey more manageable. In this live roundtable, SherpaPharma users will share real-world insights into EM digitalization.
No slides, no presentations, just candid perspectives from advanced therapy manufacturers and contract labs who have implemented SherpaPharma in highly regulated environments.
Digital transformation in pharmaceutical quality systems can be complex but the right tools and partnerships can make the journey more manageable. In this live roundtable, SherpaPharma users will share real-world insights into EM digitalization.
- Challenges prior to SherpaPharma implementation
- Key drivers and decision-making process for choosing SherpaPharma
- Making the financial business case to leadership
- Implementation experience
- Tangible results and operational improvements post-implementation
No matter where you are in your digitalization journey- whether you’re just imagining the possibilities, knee-deep in implementation, or already reaping the rewards-this session offers valuable takeaways to support your transformation.
The event is free, but registration is required. Register now to watch the webinar.
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Donald François
Senior Manager QC Microbiology
Rocket Pharmaceuticals
Donald Francois is Senior Manager of QC Microbiology at Rocket Pharmaceuticals, where he leads contamination control strategies, EM programs, and method validation for advanced biologics. With over 15 years of experience in pharmaceutical quality and lab operations, he has worked across leading companies like Novartis, Sanofi Pasteur, and Ferring Pharmaceuticals.
Donald has deep expertise in aseptic processing, cleanroom qualification, microbial ID, and sterilization validation. He’s also served as SME in audits, led Lean Lab initiatives, and contributed to facility design projects. A strong advocate for data integrity and quality culture, he is also a certified ALCOA+ trainer.
Aung Lwin
Senior Director Quality Control
Artiva Biotherapeutics
Aung Lwin a Senior Director of Quality Control at Artiva Biotherapeutics in San Diego, California. Aung is a biologist with over 20 years’ experience in the life sciences and biotech industries. He has extensive knowledge in analytical development and drug development and managing and operating Quality Control laboratories in highly regulated GMP settings.
He is currently head of Quality Control at Artiva Biotherapeutics; a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies.
Paul Lutz
Senior Director Quality Control
Focus Laboratories
Paul Lutz is a seasoned validation and regulatory expert with a decade of experience in pharmaceutical quality and compliance. As Director of Environmental Monitoring at Cormica’s Focus Labs, he has led large-scale EM programs, managed complex EMPQ implementations, and advised companies globally on best practices for microbial control.
Paul’s practical insight into trending, risk management, and regulatory audits positions him as a leading authority in the contract lab space.
Hosted by:
Alexandra Bezilla
SherpaPharma PM & Technical Specialist
Having contributed significantly to industry leaders such as Lonza, Qiagen, Roosterbio, Emergent Biosolutions, and CBMG, Alex brings a blend of technical acumen with hands-on expertise. As a career QC scientist and growing compliance expert, she has consistently demonstrated a commitment to operational excellence and continuous improvement.
Alex holds an undergraduate degree in Biochemical Engineering from UMBC and a graduate degree in Biomedical Engineering from Clemson University. Beyond the laboratory, she brings a global perspective, having lived abroad in China, and is fluent in Mandarin Chinese. Alex also enjoys rock climbing and indulges in tabletop gaming.