Industries like pharmaceuticals, biotechnology and food and beverage, compliance and operational efficiency are paramount.
In this webinar, the expert speakers will focus on a no/low-code good manufacturing practice (GMP) laboratory information management system (LIMS) that enables labs and manufacturers
to meet the rigorous demands of compliance, quality, environmental standards and scalability in a unified platform.
The expert speakers will focus on the following topics:
- Elevating Quality and Compliance: How compliance with 21 CFR Part 11 and EU Annex 11 streamlines processes such as quality control, environmental monitoring and stability management
- Adapting to Change with Flexibility: How a configurable, no-code platform allows for quick adjustments to meet changing regulatory requirements and project needs while maintaining compliance
- Optimizing Operational Efficiency: How features like automated workflows, batch creation, sampling plans and advanced analytics can enhance traceability, minimize errors and save valuable time
- Safeguarding Data Integrity: How robust audit trails, electronic signatures and permission-based controls help ensure data security and meet regulatory standards
This webinar focuses on advanced modules for QC LIMS, environmental monitoring and stability testing, demonstrating how the system integrates these components to optimize workflows, generate actionable insights and boost productivity while ensuring strict compliance.
Register for this webinar today to discover how a no/low-code GMP laboratory information management system (LIMS) can transform compliance, quality control and operational efficiency.
Speaker
Aaron Schooler, Senior Manager Pre-Sales, Sapio Sciences
An experienced Software Manager, Solution Architect and Engineer with a demonstrated history of working in the life sciences computer software industry. Aaron has been with Sapio for 11 years and has over these years been involved in several positions, including Solution Architect, Head of Customer Success, Sr. Mgr Pre-sales, and more.
Message PresenterWho Should Attend?
This webinar is ideal for professionals in highly regulated industries, including pharmaceutical manufacturing, clinical research, food and beverage production and environmental testing, who are looking to enhance their GMP processes with innovative technology.
What You Will Learn
Attendees will learn about:
- How CFR Part 11 and EU Annex 11-compliant solutions streamline QC, EM and stability management
- How a configurable, no-code platform enables seamless adjustments to meet new regulatory requirements and evolving project needs
- How features like automated workflows, batch creation, sampling plans and advanced analytics improve traceability, reduce errors and save time
- How robust audit trails, electronic signatures and permission-based controls ensure data security and regulatory compliance
Xtalks Partner
Sapio Sciences
Sapio Sciences’ mission is to improve lives by accelerating discovery, and because science is complex, Sapio makes technology simple. Sapio is a global business offering an all-in-one science-awareTM lab informatics platform combining cloud-based LIMS, ELN, and Jarvis data solutions.
Sapio serves some of the largest global and specialist brands, from biopharma research and development to clinical and diagnostic labs and manufacturing, including NGS genomic sequencing, bioanalysis, bioprocessing, chemistry, stability, histopathology, and in vivo studies.
Customers love Sapio’s platform because it is robust, scalable, and with no-code configuration, can quickly adapt to meet unique needs.
For more information, visit www.sapiosciences.com and follow us on LinkedIn.
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