by ramesh | Mar 6, 2023 | Pharmaceutical Guidance
Quality Control Documents, in short, QC Documents are essential requirements in order to maintain compliance at the QC department. Quality documents are categorized into different forms based on the requirements. Refer below to the short names, full form, definitions...
by ramesh | Mar 6, 2023 | Chromatography Troubleshooting
Ghost Peaks in HPLC (Liquid Chromatography) are a common issue in Analytical Laboratories. Image Courtesy Agilent Handling of Ghost Peaks in HPLC The Ghost peaks in Liquid Chromatography (HPLC) are contaminant peaks that may appear even when no sample is injected....
by ramesh | Mar 6, 2023 | Pharmaceutical Guidance
OOS SOP is a basic requirement in the pharma industry to investigate Out of Specification (OOS) results. Introduction of OOS SOP “Out Of Specification” (OOS) result investigation is a key GMP requirement in Pharmaceutical Industry. Hence, Out of...
by ramesh | Mar 6, 2023 | Analytical Chemistry
Solution Preparation is a key aspect in the field of Pharmaceutical Analytical Laboratory (Quality Control). Because the Solution preparation will decide the accurate results. Image Courtesy Canva Pro Techniques for Solution Preparation Based on the sample solution...
by ramesh | Mar 5, 2023 | Pharmaceutical Guidance
Electrogravimetry is one of the most important parts of Quantitative Chemical Analysis. Introduction of Electrogravimetry Analysis Electrogravimetry uses to determine the elements by depositing them electrolytically upon a suitable electrode. Filtration is not...
