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In Pharmaceutical and Biopharmaceutical manufacturing industries, per ASTM E 2500, as a part of operations & continuous improvement, qualified systems ...
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System safety System Safety is the application of engineering and management principles, criteria, and techniques to optimize all aspects of ...
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Any project is successful when the right team works on it. For any construction or renovation project an MEP consulting ...
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If you are involved in any type of manufacturing that is regulated by the FDA, FDA regulatory consulting firms can ...
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Distillation is used to separate components in a feed mixture based upon their relative boiling points. A simple, continuous distillation ...
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RO/DI stands for Reverse Osmosis and Deionization. The product is a multi-stage water filter, which takes in ordinary tap water ...
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Typically used in manufacturing or scientific research, a cleanroom is a controlled environment that has a low level of pollutants ...
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Pinch Point Analysis is a systematic process design methodology consisting of a number of concepts and techniques that ensure an ...
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Tips and tricks for getting the most out of Clean in Place/Sterilization in Place results Regardless of whether or not ...
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Any project that is within the fields of engineering or construction will come a high level of risk. It is ...
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Many people interchange hazard and risk on a daily basis. Unfortunately, they are actually two different concepts. The difference may ...
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In today’s industrial age, where manufacturing processes are highly crucial and a synonym of development and growth, the need to ...
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The Good Automated Manufacturing Practice (GAMP) Forum was founded in 1991 by pharmaceutical industry professionals in the United Kingdom to ...
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From conducting Feasibility studies, FEED / Basic & Detail engineering during the engineering phase to providing field engineering services during ...
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The pharmaceutical sector is governed by regulatory norms to ensure that quality standards are met for products in line with ...
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Validation is a critical tool to assure the quality of computer system performance. Computer system software validation increases the reliability ...
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Pharmaceutical manufacturing is a highly regulated industry. Given the stress on product quality and the widespread impact of substandard production ...
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A Validation Master Plan or a VMP is a document that outlines the principles and defines which processes and equipment ...
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For pharmaceutical industries, product quality is paramount. Minor inconsistencies can lead to major disasters. To maintain quality assurance, consistency and ...
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Water is the one of the major commodities used by the pharmaceutical industry. It is widely used as a raw ...
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Temperature mapping is important for verifying the efficacy of temperature controlled storage systems such as cool rooms, fridges and warehouses ...
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What is clean steam? Clean steam is used in the pharmaceutical and healthcare industries in processes where the steam or ...
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Irrespective of its occupancy status, a fire can happen at any time and any place. Fire has the potential to ...
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“An ounce of prevention is worth a pound of cure.” As this old saying goes, safety should be an important ...
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Detailed engineering are studies which creates a full defined scope of work for every aspect of project development. It is ...
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For the Pharmaceutical industry, validation of processes and equipment is crucial; while the FDA doesn’t necessarily demand one, documented evidence ...
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Chemical and Pharmaceutical Plant Construction projects involve high risks and heavy investments. Sometimes a single risk can manage to blowout ...
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Urban water reuse is a term generally applied to the use of reclaimed water for the beneficial irrigation of areas ...
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HVAC (stands for Heating, Ventilation and Air Conditioning) equipment needs a control system to regulate the operation of a heating ...
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A company contracted for Basic engineering design package adapts it according to the chosen scope of supply work, ranging from ...
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In a highly competitive global economy, maximizing results by eliminating costly inefficiencies is critical. Chemical & Process Industries in India ...
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When you embark on a fire pump design in India, one of the most important things to consider is your ...
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All Pharma validation services companies provide a comprehensive validation service at every stage of the project life cycle. These companies ...
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A respected tool for achieving energy efficiency is process heat integration with pinch analysis. This article presents an overview on ...
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Waste minimization is essential for every industry that manufactures products and incurs cost. In India alone, there are a large ...
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The design and engineering of equipment involves a huge amount of factors from inception to completion. Managing a large project ...
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