by maheshbhuva | May 17, 2025 | Analytical Chemistry, Analytical method development hplc,, Method validation, QMS, Quality control (QC), Wheat
According to the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guideline Q2(R1), specificity is defined as:”Specificity is the ability to assess unequivocally the analyte in the presence of components...
by maheshbhuva | May 5, 2025 | Analytical Chemistry, Analytical method development hplc,, Method validation, Pharmaceutical interview,, Quality control (QC), stability
Ah, method validation planning in pharma – a cornerstone of ensuring the quality and reliability of pharmaceutical products! It’s all about demonstrating that your analytical methods are fit for their intended purpose.To get started with effective method...
by maheshbhuva | Mar 24, 2025 | Hplc, Quality control (QC)
Share this: Click to share on Facebook (Opens in new window) Facebook Click to email a link to a friend (Opens in new window) Email Click to share on Reddit (Opens in new window) Reddit More Click to share on X (Opens in new window) X Click to share on LinkedIn (Opens...
by maheshbhuva | Feb 20, 2025 | Hplc, Hplc column
1) Partial Blockage of column 2) Adsorption of sample impurities inside column surface. 3) Poorly packed stationary phase. 4) Mechanical or thermal shocks during Handling. 5) Chemical attack on the stationary phase. Share this: Click to share on Facebook (Opens in new...
by maheshbhuva | Feb 19, 2025 | Hplc
1. What is HPLC? Answer:HPLC stands for High-Performance Liquid Chromatography. It is a technique used for separating, identifying, and quantifying components in a mixture. It uses a liquid mobile phase under high pressure to pass through a column containing a...
