Industries like pharmaceuticals, biotechnology and food and beverage, compliance and operational efficiency are paramount.
In this webinar, the expert speaker 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 speaker 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 LIMS can transform compliance, quality control and operational efficiency.
Keywords: Drug Development, CRO, Regulatory, Laboratory Testing, Analytical Testing, Laboratory Technology, Bioanalytical Testing, Laboratory Software, Laboratory Automation, Quality