Analytical Precision
Operational Excellence
Quality and Compliance
AV Analytics operates with controlled laboratory procedures, documented methods, and a focus on data integrity and traceability. Our facility is designed to meet the rigorous demands of pharmaceutical research market testing, ensuring every result is anchored in verifiable scientific practice.
ISO Certification Pending
Our Commitment to Analytical Quality
AV Analytics maintains the highest degree of data integrity through standardized instrument qualification and rigorous maintenance schedules. Our operations are governed by documented test methods, thorough data review, and a robust sample traceability system that ensures unique sample identification and controlled certificate-of-analysis generation. We prioritize personnel training, strict confidentiality, and continuous quality-system development to foster an environment of analytical excellence and ongoing improvement. AV Analytics is developing its quality system in alignment with recognized analytical laboratory practices and applicable ISO/IEC 17025 principles.
Quality Assurance Protocols
The laboratory workflow at AV Analytics follows a rigorous sequence of quality checks to ensure every sample is processed with scientific precision and complete traceability.
01
Sample Receipt
Visual inspection for container integrity and temperature compliance upon arrival.
02
Secure Logging
Unique sample identification and entry into documented laboratory tracking systems.
03
Controlled Storage
Samples are held under monitored environmental conditions to preserve chemical stability.
04
Analytical Testing
Execution of documented test methods using qualified instrumentation and reagents.
05
Data Review
Peer or supervisor verification of raw data, calculations, and analytical finding accuracy.
06
Reporting
Generation of controlled Certificates of Analysis and technical reports for client delivery.