Category: QC

Learn how Good Chromatography Practices enhance data integrity, ensure compliance, and boost efficiency in pharmaceutical labs for reliable, safe product outcomes.

Learn how to detect, manage, and investigate Out-of-Trend (OOT) results in pharma to maintain product quality, ensure GMP compliance, and prevent OOS issues.

Explore the impact of toxic solvents in Reversed Phase Chromatography, their risks, and eco-friendly alternatives to ensure safe, accurate testing in pharmaceutical QC labs while minimizing environmental hazards.

Discover the key differences between RP-HPLC and NP-HPLC. Learn how these contrasting chromatography techniques drive effective compound separation and analysis for diverse applications.

Discover the best practices for establishing and managing expiry dates for commercial and in-house prepared reagents in QC labs.

Discover the importance of IQ, OQ, and PQ in GMP, ensuring equipment and systems are installed and function correctly to maintain high-quality manufacturing standards.

Ensuring data integrity and governance in GMP: a comprehensive guide to accurate, consistent, and reliable data management practices for pharmaceutical professionals.

Discover essential tips for calibration, handling, and maintenance of pH meters in QC labs.

Ensure precision in QC labs with proper calibration and performance checks of analytical balances. Learn best practices for reliable and compliant results.

Learn more about Batch Manufacturing Records (BMR), essential for consistent, safe pharmaceutical production and compliance with regulatory standards.