by maheshbhuva | May 28, 2026 | 483 observation, ALCOA++, Analytical method development hplc,, Hplc, Job interview, News Pharma, Pharmaceutical interview,
STEP-BY-STEP PROCEDURE 1. PURPOSE To describe the steps for initiation, investigation, implementation, effectiveness check and closure of Corrective and Preventive Actions (CAPA) in QMS to ensure product quality and compliance with regulatory requirements. 2. SCOPE...
by maheshbhuva | May 16, 2026 | Hplc, Hplc column, HPLC VIAL, Job interview, Pharmaceutical interview,, Quality control (QC)
In the competitive landscape of modern pharmaceutical companies, ensuring precise product quality isn’t just a regulatory requirement—it is the foundation of patient safety. At the heart of this quality assurance is HPLC analysis (High-Performance Liquid...
by maheshbhuva | Nov 3, 2023 | 21 CFR, Uncategorized
21 CFR stands for Title 21 of the Code of Federal Regulations. It is a set of regulations issued by the United States Food and Drug Administration (FDA) that covers various aspects of regulatory requirements for pharmaceuticals, medical devices, food, cosmetics, and...
by maheshbhuva | Jul 25, 2023 | Glassware
The terms “Class A” and “Class B” are commonly used to describe different types of glassware in laboratory settings, particularly for volumetric measuring. These classes have specific standards and tolerances, and they serve different purposes....
by maheshbhuva | Jul 25, 2023 | Glassware
Laboratories use various types of glassware to perform experiments, conduct measurements, and handle substances safely. Some common types of glassware used in laboratories include: Beakers: Cylindrical containers with a flat bottom and a spout used for holding and...
