The industry standard in automated SQC workflow

Precision I&MR Charts, Q-Charts, EPA 0.75R, and pretreated accuracy charts (Case 1 and Case 2) are built directly into the SQC+ workflow. Your team works within a structure that reflects the standard, reducing interpretation errors and ensuring consistent methodology across analysts and locations.

SQC+ simplifies historic data export for EPA NSTOP and generates attestation reports without manual compilation. What typically requires hours of data gathering and formatting is reduced to a straightforward, repeatable process that holds up under regulatory scrutiny.

Control limit evaluation and update processes are aligned with ISO 4259 requirements. Labs operating under both ASTM and ISO frameworks can maintain a single, unified QC workflow rather than managing parallel processes or separate documentation systems.

Every QC event, corrective action, user entry, and system change is recorded in a full, revisable audit database. When audits occur, your team is not scrambling to reconstruct records; the documentation is already complete and organized.

QC samples are automatically logged and scheduled based on configured QC business logic, eliminating manual tracking and reducing the risk of missed or delayed samples. Lab personnel follow a consistent, system-driven schedule rather than relying on individual memory or manual coordination.

Out-of-control signals trigger automated alerts delivered to responsible personnel via email or mobile device, 24 hours a day. QC leads are notified immediately when action is required, regardless of whether they are on the floor or off-site.

When an out-of-control condition is detected, recheck samples are auto-logged and affected instruments are held from use until the corrective action workflow is complete. This prevents non-conforming results from passing through to product certification.

Periodic control limit evaluation is guided by visual dashboard indicators, simplifying a process that often requires significant statistical expertise. SQC+ surfaces the data and context needed for informed decisions without requiring analysts to work outside the system.

Enterprise-wide dashboards provide a consolidated view of QC status across multiple labs, sites, or organizational units. Quality managers can identify performance gaps and trends at the site or enterprise level without requesting reports from individual locations.

Monthly, quarterly, and annual reviews compare site precision against individual analyst contributions and results. This data supports objective performance conversations and helps identify training needs before they become compliance issues.

Common causes of variation are identified and ranked across instruments, methods, and materials. This structured view of recurring issues allows QC teams to prioritize corrective action where it will have the greatest impact on lab performance.

When deployed alongside BLISS on the single Baytek platform, real-time instrument capability data is accessible within the LIMS. Instruments that fall out of control can be flagged to stop COA certification automatically, preventing non-conforming results from reaching the customer.