
TPL’s six-layer architecture enables regulated multi-site laboratory organizations—regardless of industry or location—to maintain consistent practices across states and countries through a centralized hub.
This single source of truth makes policies and activities easy to share while capturing results for ready access and visibility.
Master SOPs, training, competency and workflow templates for every lab and testing discipline you operate.
Maintain controlled master content and versioning for each of your lab sites.
Distribute approved SOPs, training, competency requirements, quality expectations, sample handling and transfer data, and workflow templates across sites.
Share standardized documents and workflows between sites and organizations.
Local teams perform assigned workflows and capture bench-level evidence, from training and competency assessments to instrument and method QC.
Enable staff to complete tasks, forms, checks, training and quality activities within TPL.
Manage proficiency testing, QC, deviations, CAPA, quality reviews, document approvals and audit-ready evidence.
Turn daily lab activity into audit-ready records aligned with your accreditation and regulatory requirements.
Give operations, quality and leadership teams visibility and access to every accreditation, audit and compliance activity.
Enable permission-based access across sites and organizations.
Reduce manual data duplication and improve aggregation of quality data, such as sample traceability and turnaround times, from fragmented systems of record, laboratory information systems, middleware and instruments.
TPL enables API integrations, data abstraction, reporting, and metrics across multiple sources.

See the few steps needed to implement the TPL platform and simplify operations while boosting quality and compliance in your lab.