Through continuous upgrades in technology, training, and compliance, we remain committed to maintaining the highest standards of pharmaceutical quality control—ensuring that every product leaving our facility is of consistent Quality, safe and effective.
Quality Control: Precision, Compliance & Excellence
At Blue Cross Laboratories, Quality Control is the backbone of our commitment to delivering safe, effective, and high-quality pharmaceutical products. Our state-of-the-art Quality Control (QC) laboratories, staffed by highly skilled professionals in Pharmacy, Chemistry, Microbiology, and Analytical Sciences, ensure that every product meets stringent national and international regulatory requirements. Through a combination of advanced technology, validated analytical methods, and rigorous compliance protocols, we uphold our promise of delivering pharmaceuticals of unmatched safety, purity, and efficacy.
Cutting-Edge Quality Control Laboratories
Our modern Quality Control facility comprises dedicated Chemical, Instrumental, and Microbiology laboratories, each equipped with sophisticated, industry-leading instruments such as: - High-Performance Liquid Chromatography (HPLC) for precise analysis of Pharmaceuticals and related compounds - Fourier Transform Infrared Spectroscopy (FTIR) for molecular identification - Gas Chromatography (GC) for volatile compound analysis - UV-Visible Spectrophotometers for Spectrophotometric analysis of Pharmaceuticals - Dissolution Testers for in-vitro drug release evaluation - Total Organic Carbon (TOC) Analyzers for ensuring purity of purified water - Walk-in humidity chambers to ensure stability of products till their shelf life To ensure error-free and consistent performance, all instruments undergo rigorous calibration and validation at regular intervals.
Validated Analytical Methods & Stability Studies
We adhere to WHO and ICH Q2 guidelines for analytical method validation, ensuring accuracy, specificity, precision, and robustness in our testing procedures. Method Validation: Our validated analytical techniques ensure that all tests produce reliable and reproducible results. Stability Studies: Following ICH Q1 guidelines, we conduct extensive stability studies under various environmental conditions to confirm that our products maintain their potency, safety, and efficacy throughout their shelf life.
Stringent Laboratory Compliance & Data Integrity
Pharmacopoeia-Defined Standards: Our product specifications align with global pharmacopoeial standards (USP, BP, IP) and rigorous in-house test parameters. Regulatory Compliance: Every test is performed following validated Standard Testing Procedures (STP), ensuring compliance with Good Laboratory Practices (GLP) and national and international regulatory bodies. Data Integrity & Documentation: All laboratory data is meticulously recorded, reviewed, and protected, ensuring full traceability, accuracy as per ALCOA++, and regulatory compliance.
Chemical Lab
Microbiology Lab
