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QC Analytical Lab Testing

Analytical Quality Control Fundamentals provides a foundational introduction to the essential laboratory practices that underpin Quality Control (QC) operations in pharmaceutical and biopharmaceutical environments. Designed for those new to QC testing or seeking to strengthen their understanding of core analytical principles, this course explores not only what happens in the QC laboratory, but why these practices are vital for ensuring product quality, regulatory compliance, and ultimately, patient safety.

Through practical examples and structured guidance, learners will gain insight into the complete QC analytical testing workflow—from sampling and instrument qualification to system suitability, data integrity, and regulatory expectations such as ICH Q6A. The course also emphasizes the critical connection between accurate, reliable laboratory data and timely product release decisions, reinforcing how robust QC practices support consistent GMP manufacturing.

By the end of this course, participants will understand the scientific principles, operational workflows, and good documentation practices necessary to ensure reliable QC testing results. They will be equipped to apply best practices in data integrity, record‑keeping, and laboratory operations that contribute to a resilient and compliant Pharmaceutical Quality System (PQS).
300.00