WATER SYSTEM IN PHARMACEUTICAL INDUSTRY
PREFILTRATION: – The purpose of prefiltration—also referred to as initial, coarse, particulate, or depth filtration—is to remove solid contaminants from the incoming source water…
Category: Pharma Manufacturing
ROUGING PHENOMENA IN PHARMACEUTICAL WATER SYSTEM
Rouging is seen in many water systems, usually high temperature (80°C) distilled water and clean steam systems. Rouge is not limited to storage and…
GLASS: PACKAGING MATERIAL USED IN PHARMA
American Society for Testing and Materials (ASTM) defines glass as an inorganic product of fusion that has cooled to a rigid condition without crystallizing. ASTM…
ACIDIFICATION/DEGASIFICATION PROCESS OF WATER SYSTEMS IN PHARMA
The process is well known and accepted in water purification systems. It is usually used where there is a high flow rate (>50 gpm…
CLASSIFICATION OF MILLS USED IN PHARMA INDUSTRY
The majority of size reduction equipment may be classified according to the way in which forces are applied namely; impact, shear, attrition, and shear-compression. A…
SAP (SYSTEMS, APPLICATIONS, PRODUCTS IN DATA PROCESSING) IN PHARMACEUTICAL INDUSTRY
Introduction:- SAP system allows a company to share common data and practices across the enterprise and produce and access information in a real time environment…
PERSONNEL TRAINING FOR PHARMACEUTICAL INDUSTRY 3
INTRODUCTION:- The pharmaceutical industry is facing a tremendous changes and challenges nowadays. It has been observed that lack of proficient, talented, capable employees has enforced…
DIFFERENCE BETWEEN FUMIGATION AND FOGGING PROCESS
Fumigation and fogging are two methods commonly used in pharmaceutical companies to control the microbial contamination in controlled area. But now a day’s fumigation of…
TEST METHOD FOR PRESSURE DIFFERENTIALS IN ASEPTIC DISPENSING FACILITIES
Introduction:- The test defined here is an independent check on the accuracy of any continuous monitoring system. It is likely that the test as defined…
TEST METHOD FOR AIR CHANGE RATE (ACR) IN ASEPTIC DISPENSING FACILITIES
Introduction:- Conventional clean rooms operate on the principle that the air supplied to the room is of sufficient quantity to dilute or remove the contamination…
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