Displaying items by tag: design

In order to protect consumers, United States pharmaceuticals are one of the most heavily regulated industries in the country. The FDA creates a number of standards and tests for Pharma companies to comply with in order to create new drugs and manufacture current ones to reduce side effects and ultimately mitigate the risks to their customers. And creating a highly controlled, uncontaminated manufacturing and packaging environments is a high priority. Pharmaceutical cleanrooms are specially designed to produce this environment.

First, you must determine if a clean room is necessary. Cleanrooms are designed to maintain extremely low levels of particulates. These particulates can cause damage to sensitive items such computer components, Semiconductor fabrications, solar panels, batteries, and other sensitive products. They can come in many sizes and can even encompass entire manufacturing facilities depending upon the products being manufactured there. Contaminants, such as dust, and other airborne organisms can cause irreparable damage to these products, and cleanrooms are designed to defend against such contaminants. They are built specifically to manage and maintain a specific level of particulates that would not harm these products and typically have a cleanliness level quantified by the number of particles per cubic meter.

Designing a cleanroom is a meticulous and precise process that demands careful planning and attention to detail. The goal is to create an environment that meets specific purity standards essential for various industries, such as pharmaceuticals and aerospace.

Building an extra building next to your office factory will take you longer. For this reason cleanroom have become than erecting a worthwhile investment in terms of creating space for your goods and supplies.

Need to design a cleanroom? With an increasing emphasis on maximizing product yield, improving quality control and ensuring safety, more companies than ever are looking to install cleanrooms and controlled environments in their facilities.  This article is designed to answer the commonly asked question, "How do I design a cleanroom?"

This quick clean room design checklist is part of a number of free suggestions, tools or tips put together by our (frustrated) staff to try circumvent a poor clean room design.

Optimize your space and increase productivity with a properly laid-out cleanroom design. Creating a cleanroom that is productive and efficient requires a large amount of planning. The purpose of the cleanroom you are designing, the number of people working in the area, and the best way to make the most of your space are essential aspects in creating a highly functional cleanroom.

ISO 8 cleanroom design requires the understanding of several methodologies and procedures that evaluate airborne contamination levels including ISO 14644-1 to ISO 14644-8, ISO 14698-1, and ISO 14698-2.

Planning a cleanroom can be an overwhelming task! From site selection to calculating airflow changes and MEP requirements to clash coordination and onsite execution, there are no minor details. To hit your key dates for turnover and validation, your team needs to have an organized plan from the beginning. Below you will find helpful considerations, tips, and guides for designing and building your next cleanroom project.

Cleanrooms and controlled contamination environments are increasingly being used across many industrial sectors, including the pharmaceutical industry. An important issue is the operating cost associated with cleanroom energy consumption and, consequently, the identification of applicable energy containment measures. This article reviews pharmaceutical cleanroom calculations for non-unidirectional airflow against energy consumption with known sources of contamination and type of air diffusion used. It proposes alternative cases to compare potential economic savings from applying energy-saving measures proposed by ISO 14644-16.1