Blog

In Pharmaceutical and Biopharmaceutical manufacturing industries, per ASTM E 2500, as a part of operations & continuous improvement, qualified systems ...

System safety System Safety is the application of engineering and management principles, criteria, and techniques to optimize all aspects of ...

Any project is successful when the right team works on it. For any construction or renovation project an MEP consulting ...

If you are involved in any type of manufacturing that is regulated by the FDA, FDA regulatory consulting firms can ...

Distillation is used to separate components in a feed mixture based upon their relative boiling points. A simple, continuous distillation ...

RO/DI stands for Reverse Osmosis and Deionization. The product is a multi-stage water filter, which takes in ordinary tap water ...

Typically used in manufacturing or scientific research, a cleanroom is a controlled environment that has a low level of pollutants ...

Pinch Point Analysis is a systematic process design methodology consisting of a number of concepts and techniques that ensure an ...

Tips and tricks for getting the most out of Clean in Place/Sterilization in Place results Regardless of whether or not ...

Any project that is within the fields of engineering or construction will come a high level of risk. It is ...

Many people interchange hazard and risk on a daily basis. Unfortunately, they are actually two different concepts. The difference may ...

In today’s industrial age, where manufacturing processes are highly crucial and a synonym of development and growth, the need to ...

The Good Automated Manufacturing Practice (GAMP) Forum was founded in 1991 by pharmaceutical industry professionals in the United Kingdom to ...

From conducting Feasibility studies, FEED / Basic & Detail engineering during the engineering phase to providing field engineering services during ...

The pharmaceutical sector is governed by regulatory norms to ensure that quality standards are met for products in line with ...

Validation is a critical tool to assure the quality of computer system performance. Computer system software validation increases the reliability ...

Pharmaceutical manufacturing is a highly regulated industry. Given the stress on product quality and the widespread impact of substandard production ...

A Validation Master Plan or a VMP is a document that outlines the principles and defines which processes and equipment ...

For pharmaceutical industries, product quality is paramount. Minor inconsistencies can lead to major disasters. To maintain quality assurance, consistency and ...

Water is the one of the major commodities used by the pharmaceutical industry. It is widely used as a raw ...

Temperature mapping is important for verifying the efficacy of temperature controlled storage systems such as cool rooms, fridges and warehouses ...

What is clean steam? Clean steam is used in the pharmaceutical and healthcare industries in processes where the steam or ...

Irrespective of its occupancy status, a fire can happen at any time and any place. Fire has the potential to ...

“An ounce of prevention is worth a pound of cure.” As this old saying goes, safety should be an important ...

Detailed engineering are studies which creates a full defined scope of work for every aspect of project development. It is ...

For the Pharmaceutical industry, validation of processes and equipment is crucial; while the FDA doesn’t necessarily demand one, documented evidence ...

Chemical and Pharmaceutical Plant Construction projects involve high risks and heavy investments. Sometimes a single risk can manage to blowout ...

Urban water reuse is a term generally applied to the use of reclaimed water for the beneficial irrigation of areas ...

HVAC (stands for Heating, Ventilation and Air Conditioning) equipment needs a control system to regulate the operation of a heating ...

A company contracted for Basic engineering design package adapts it according to the chosen scope of supply work, ranging from ...

In a highly competitive global economy, maximizing results by eliminating costly inefficiencies is critical. Chemical & Process Industries in India ...

When you embark on a fire pump design in India, one of the most important things to consider is your ...

All Pharma validation services companies provide a comprehensive validation service at every stage of the project life cycle. These companies ...

A respected tool for achieving energy efficiency is process heat integration with pinch analysis. This article presents an overview on ...

Waste minimization is essential for every industry that manufactures products and incurs cost. In India alone, there are a large ...

The design and engineering of equipment involves a huge amount of factors from inception to completion. Managing a large project ...