Our Bioanalytical Laboratory is a core component of Glocare Labs clinical research infrastructure, designed to deliver precise, reliable, and regulatory-compliant analysis of drug concentrations in biological matrices.
Capabilities & Features:
- State-of-the-art LC-MS/MS systems for high-sensitivity quantitative analysis
- HPLC system for method development and sample processing
- Validated methods for a wide range of analytes across plasma, serum, urine, and other biological samples
- Strict adherence to Good Laboratory Practice (GLP) and regulatory guidelines (CDSCO, USFDA, EMA)
Facilities Include:
- Dedicated sample processing and extraction areas
- Controlled temperature sample storage rooms (refrigerators and deep freezers with temperature monitoring)
- Stability chambers for sample integrity testing under various conditions
- Secure data acquisition and storage systems ensuring traceability and audit readiness
Expert Team:
- Experienced bioanalytical scientists, method developers, and QA personnel
- In-house capability for method development, validation, and transfer
Proficient in handling complex matrices and challenging analytes