Revolutionizing Pharma QC under GMP
reduction in FTE costs
reduction in time to business
Sciquoia is transforming pharmaceutical quality control with cutting-edge automation solutions. By automating GMP-regulated lab processes, we improve precision, reduce human error, and ensure compliance. Our advanced approach streamlines QC workflows, making them faster, more efficient, and scalable, driving the future of drug manufacturing.
Benefits
Sciquoia's approach enables significant benefits if compared to manual work or vs. state of the art automation with open systems
vs. manual work
Reduces full-time employees (FTEs) by 50% in routine use
Enables break-even within 1.5 - 2 years
Decreases deviations in routine use by 65%
vs. an open system
Accelerates time to business from 18 to 4 months
Cuts CapEx and implementation cost by 50%
Simplifies technology transfer
Sciquoia's Unique Approach
Sciquoia is transforming GMP-regulated QC automation with pre-qualified, off-the-shelf workflow solutions under GAMP 5 Category 4. Our approach blends flexible method development with pre-qualification to ensure reliable performance, streamline compliance, and accelerate implementation. Designed for ease of use in routine operations, our systems enhance productivity and reduce errors. Seamless integration with digital platforms like LIMS guarantees full traceability, positioning Sciquoia as the optimal choice for regulated QC environments.
