This article describes about Purified Water System Qualification in the Pharmaceutical Industry. Purified Water System Qualification in the Pharmaceutical Industry: A Complete Guide Introduction Water is one of the most critical raw materials used...
Equipment Qualification in Pharma: Ensuring Compliance, Accuracy, and Product Quality Introduction In the pharmaceutical industry, equipment qualification in pharma is a vital component of Good Manufacturing Practice (GMP) compliance. It ensures that every piece of...
Freeze Thaw Study in Pharmaceuticals: A Critical Stability Testing Tool Introduction In pharmaceutical development and quality control, stability testing plays a critical role in ensuring that a drug product maintains its safety, efficacy, and...
ICH Stability: The Global Standard for Drug Shelf Life and Quality Assurance Introduction One of the most trusted frameworks for evaluating the stability of pharmaceutical products is the ICH stability guidelines, issued by the...
Accelerated Stability Testing in Pharmaceuticals: Fast-Tracking Product Shelf Life Evaluation Keywords: accelerated stability testing, pharmaceutical stability studies, ICH guidelines, shelf life prediction, drug stability testing, pharmaceutical quality assurance Introduction In the pharmaceutical industry, ensuring...
This article contains about 10 Steps to ensure accurate HPLC Results 10 Steps to ensure accurate HPLC Results High-Performance Liquid Chromatography (HPLC) is a powerful analytical technique widely used in pharmaceuticals, environmental testing,...
This article describes about (Standard Operating procedure) SOP on Entry and Exit procedure for microbiology section in Pharmaceutical Industry. SOP on Entry and Exit procedure for Microbiology section I. Purpose & Scope: To provide...
This article describes about what must be done when Transfer of Material/Equipment in Aseptic area. Transfer of Material/Equipment in Aseptic area What can be done when materials and/or equipment are being transferred into a...
This articles contains information about Cpk (Process Capability Index) and Why CpK greater than 1.33 is considered acceptable Why CpK greater than 1.33 is considered acceptable The Cpk (Process Capability Index) is a statistical measure...
This article contains information about Desiccator – A Quality control Laboratory Device which is used in the Quality control laboratory used to maintain the dryness of samples by removing moisture from an enclosed space. Desiccator –...