Data Security - Pharmaguidelines

“Ensuring Excellence: The Crucial Role of Data Integrity in Pharmaceutical Manufacturing”

Leave a Comment / Blog / pharmaguidelines.co.uk

1. Understanding Data Integrity Data integrity refers to the accuracy, completeness, and consistency of data throughout its lifecycle. It ensures that data, whether in electronic or paper-based formats, is reliable and trustworthy. In the pharmaceutical industry, this includes manufacturing records, laboratory test results, and quality assurance documentation. 1.1 ALCOA+ Principle The ALCOA+ principle underpins data […]

“Ensuring Excellence: The Crucial Role of Data Integrity in Pharmaceutical Manufacturing” Read More »

Best Practices for Documentation in HPLC Method Development

Documenting the HPLC (High-Performance Liquid Chromatography) method development process is not only a good practice but also an essential requirement for ensuring the reproducibility, reliability, and compliance of analytical methods. In this article, we explore the best practices for documentation in HPLC method development, shedding light on the importance of comprehensive and organized records throughout