Sample Preparation

Standard Operating Procedure (SOP) for Laboratory Investigation Procedure

Standard Operating Procedure on Laboratory Investigation Procedure

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“Discover the systematic approach to conducting laboratory investigations with precision and accuracy through this comprehensive Standard Operating Procedure (SOP). Learn about sample collection, preparation, analysis, data interpretation, and safety protocols for ensuring reliable results.”

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Standard Operating Procedure (SOP) for Stability Chamber Management

Standard Operating Procedure for Stability Chamber Management

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A comprehensive Standard Operating Procedure (SOP) for Stability Chamber Management, detailing procedures for setup, sample preparation, chamber operation, monitoring, data recording, deviations, documentation, training, and compliance. Essential for ensuring accurate stability testing of products.

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USGS scientist operating a high-performance liquid chromatography (HPLC) system in a laboratory

HPLC Method Development for Environmental Analysis: Practical Guide

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HPLC method development for environmental analysis begins with a defined analyte, sample matrix and decision the data must support. A fit-for-purpose method can measure selected organic contaminants in water, soil, sediment or wastewater, but no single HPLC method detects every pollutant. This guide explains how environmental laboratories plan sample handling, separation, detection and quality controls

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USGS scientist operating a high-performance liquid chromatography (HPLC) system in a laboratory

HPLC Method Development for Pharmaceutical Analysis: A GMP Guide

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HPLC method development for pharmaceutical analysis is a planned, evidence-based process for creating a chromatographic procedure that is fit for its intended use. This guide explains how pharmaceutical QC and analytical development teams can define the method objective, select chromatographic conditions, prepare samples, evaluate performance and document decisions within the site quality system. Educational scope:

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USGS scientist operating a high-performance liquid chromatography (HPLC) system in a laboratory

HPLC Method Development: 5 Practical Steps for Pharma QC

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HPLC method development is the planned design and evaluation of chromatographic conditions so an analytical procedure can meet a defined purpose. For pharmaceutical quality control, development should produce a selective, reliable and practical method supported by documented evidence—not simply a chromatogram that looks acceptable in one trial. Educational scope: This article is a technical planning

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