Frequently Asked Questions

• Licensing and Accreditation Submission Prep
• Quality Management
• Document Control
• Process Control
• Employee Training
• Competency Assessment
• Personnel Records
• Non-Conformance Reports
• Corrective & Preventative Actions
• Complaint Handling
• QA Meeting Management
• Audit Management (Internal and External)
• Supplier Quality Management

• Early-Stage Companies:
  Startups use TPL to accelerate CLIA, FDA, and ISO submissions with guided workflows and ready-to-file compliance packets.

• Growth-Stage Companies:
  Scaling labs rely on TPL to unify quality systems, standardize SOPs, and stay audit-ready across expanding locations.

• Late-Stage & Enterprise Labs:
  Established networks leverage TPL to automate audits, manage enterprise-wide training and CAPA, and maintain global regulatory compliance.

TPL is modular and adapts to the needs of different testing organizations. We are HIPAA compliant and meet the requirements of CLIA, FDA CFR 21 Part 11, ISO 15189, ISO 9001, and common lab accrediting agencies.

The Proficient Lab standardizes SOPs, compliance processes, and operational workflows across all locations, ensuring every site runs to the same high standards. Data for all sites can be managed as one organization, as well as segmented based on needs, permissions, and working locations.

Yes, labs and testing sites can communicate, coordinate, and share data in real-time across locations, enabling teams to work together seamlessly.