GMP Analytical Testing Laboratory with Rapid Turnaround

Launching January 2026 Minnesota’s ISO 17025 Accredited, FDA-registered, DEA-licensed analytical lab specializing in pharmaceutical, and PFAS environmental testing — trusted for accuracy, compliance, and speed.

ISO AccreditedFDA RegisteredDEA RegisteredRapid Turnaround

Multi-Sector Service Categories

Comprehensive Pharmaceutical Raw Material Testing

Testing to major pharmacopeial standards (USP, EP, JP) for excipients and actives.
Advanced instrumentation—HPLC, UPLC-TQD, GC-MS, HS-GC-MS, ICP—for full analytical characterization and identity confirmation.
Rapid turnaround supporting pharmaceutical quality control, GMP compliance, and production timelines.

PFAS Environmental Testing and Regulatory Compliance

Precise detection of PFAS in water, soil, and complex environmental matrices.
Dedicated LC-MS/MS instrumentation prevents cross-contamination and ensures trace-level quantitation.
Fully aligned with Minnesota PFAS testing regulations and EPA guidelines.

Regulatory Compliance and Method Validation Services

Expert support for regulatory submissions, method development, and ICH Q2(R2) validation.
QA/QC program design ensures audit readiness, data integrity, and GMP compliance across all testing workflows.

Why Choose AYA Labs

Rapid Turnaround

Flexible scheduling, accelerated project timelines.

PhD-Level Scientists

Direct collaboration with experienced analytical chemists and regulatory experts.

Advanced Instrumentation

HPLC, GC-MS, ICP-MS, and LC-MS/MS deliver reliable, trace-level results.

Minnesota-Based Analytical Lab:

A strategic hub serving the pharmaceutical, environmental, and clinical sectors.

Comprehensive QA/QC Systems:

ISO 17025 and cGMP standards ensure reproducible, validated outcomes.

ISO 17025 AccreditationFDA RegistrationCLIA CertificationChain of Custody Procedures

Advanced Instrumentation

• LC-MS/MS for trace-level quantitation

• ICP-MS for elemental & heavy metal analysis

• GC-MS for volatiles and residual solvents

Method Validation

• Compendial methods and ICH Q2(R2) validation

• Regulatory-compliant documentation and reports

Quality Systems

• Robust QA oversight and audit readiness

• Secure data with audit trails

• COA templates tailored to your needs