Tag: cleaning validation in pharmaceutical industry

Qualification of Water Tanks, Pumps, and Distribution Loops

Qualification of Water Tanks, Pumps, and Distribution Loops Qualification of Water Tanks, Pumps, and Distribution Loops This article serves as a definitive guide for pharmaceutical professionals involved in the qualification of water tanks, pumps, and distribution loops. It rigorously outlines…

Case Study: CPP Control in Tablet Compression Process

Case Study: CPP Control in Tablet Compression Process Case Study: CPP Control in Tablet Compression Process This article serves as a practical guide for pharmaceutical professionals focusing on cleaning validation in the pharmaceutical industry, particularly in the context of a…

Risk Assessment Tools for Identifying Critical Control Points

Risk Assessment Tools for Identifying Critical Control Points Risk Assessment Tools for Identifying Critical Control Points Step 1: Understanding User Requirements Specification (URS) and Risk Assessment The foundation of a robust cleaning validation in the pharmaceutical industry begins with a…

Step-by-Step Guide to Setting Process Parameter Ranges

Step-by-Step Guide to Setting Process Parameter Ranges Step-by-Step Guide to Setting Process Parameter Ranges Establishing effective process parameter ranges is critical for the validation lifecycle within the pharmaceutical industry. This step-by-step guide focuses on specific validation tasks, documentation, data requirements,…