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 | Jul 25, 2023 | Glassware
In the pharmaceutical industry, glassware is also classified based on its quality and accuracy, much like the Class A and Class B classifications commonly used in laboratory glassware. The classification of glassware in pharma is typically based on standards set by...
by maheshbhuva | May 19, 2023 | Analytical Chemistry, stability
Chemical: Each API (active ingredient retains its chemical integrity and labeled potency within the specified limit. Physical: the physical stability properties includes appearance, palatability, uniformity, dissolution and suspend ability are retained....
by maheshbhuva | Mar 9, 2023 | stability
Stability studies are mainly of following types: • Long term stability. • Intermediate stability. • Accelerated stability. • In-use stability. Share this: Share on Facebook (Opens in new window) Facebook Email a link to a friend (Opens in new window) Email Share on...
by maheshbhuva | Jan 13, 2023 | Analytical Chemistry, Pharmaceutical interview,, Potentiometric Titration
Potentiometric titration is a laboratory method to determine the concentration of a given analyte. It is used in the characterization of acids. In this method, there is no use of a chemical indicator. Instead, the electric potential across the substance is measured....
