Category: GMP
Introduction Gap analysis is a process that compares two sets of data to identify the differences between them. In a business context, gap analysis involves examining the current state …
Introduction to Six Sigma Six Sigma is a set of techniques and tools for process improvement that seeks to improve the quality of process outputs by identifying and removing …
Introduction Qualification is an important aspect of the pharmaceutical industry that ensures quality manufacturing processes and compliant end products. It is the process of demonstrating and documenting that equipment …
Analytical weighing balances Analytical Weighing balances are most critical part of pharmaceutical industry as it directly impact the final product quality. Q1. What is the principle of analytical weighing …
Airlocks to prevent contamination Airlocks are defined as barriers between 2 controlled areas and consists of two or more than two doors meant to regulate the passage of air. Cleanroom Airlocks are …
Good manufacturing practices emerging trends GMP History dates back to 1900 and is associated with well known tragedies and actions taken to prevent them from occurring in future. In …
Degradation of Drugs in light Many drugs are prone to degrade in Presence of light. So, the impact of light on physical and chemical attributes of drug substance must be …
Temperature and Relative humidity validation Temperature and relative humidity are critical aspects of pharmaceuticals USFDA(United states food and drug administration) as well as other regulatory agencies states that we …
Deviation and Incidence Deviation and incidence in pharmaceuticals both the terms are differient with differient meanings most of pharmaceutical professionals are confused to differentiate between them when they occur. In the …
70% IPA (Iso Propyl Alcohol) In pharmaceuticals 70% IPA (Iso Propyl Alcohol) is commonly used disinfectant Mechanism of action of IPA is it enters the cell wall and dissolves the …