CIP and WIP System in Pharmaceutical Isolators

Cleanliness and sterility of various equipment are essential in the pharmaceutical industry. They ensure product safety and quality. In this regard, the CIP and WIP system in pharmaceutical isolators plays a key role in this process. In fact, it makes it possible to clean and decontaminate pharmaceutical isolators without having to dismantle them. Here is everything you need to know about this technology.

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Understanding CIP and WIP Systems in Pharmaceutical Isolators
Pharmaceutical isolators are devices that maintain a sterile environment for handling sensitive products, such as medicines or active chemicals. In order to maintain this level of sterility, it is important that these isolators are regularly cleaned and decontaminated. This is where the CIP and WIP system in pharmaceutical isolators comes into play.
The CIP or Clean In Place system is an automated process that cleans and sterilises equipment, including isolators, without the need to dismantle or move it. It uses a series of washing, rinsing and sterilisation cycles with specific solutions, usually followed by a drying cycle. It should be noted that this process ensures that all surfaces in contact with the products are cleaned effectively.
WIP, or Wash In Place, is a cleaning system that does not require complete sterilisation of various equipment. Instead, it aims to remove visible residues or potential contaminants. It is used in cases where complete decontamination is not required, but where thorough cleaning is still essential to ensure the safety and efficiency of operations.
The Advantages of Cleaning-in-Place (CIP) and Wash-in-Place (WIP) Systems
The CIP and WIP system in pharmaceutical isolators allows isolators to be cleaned quickly and efficiently without the need for disassembly. This significantly reduces downtime and improves the productivity of production processes. By automating the cleaning of isolators, this technology also minimises the risk of human error.
It ensures that all critical surfaces are cleaned uniformly, thereby reducing the risk of cross-contamination. This renowned system also complies with pharmaceutical industry standards, particularly with regard to good manufacturing practices (GMP).
More specifically, it enables compliance with the cleaning and sterility requirements imposed by health authorities. By avoiding the need for manual dismantling of isolators, it helps to save considerable time. Finally, limiting human intervention in cleaning processes reduces the risks for operators.
EREA Pharma: expert in CIP and WIP systems for the pharmaceutical industry
EREA Pharma is a leader in the supply of this system, which is specially designed to meet the requirements of the pharmaceutical industry. Drawing on our experience and expertise, we develop customised solutions that ensure the effective and safe cleaning of isolators and other equipment.
In fact, our systems offer the possibility of automating and standardising the cleaning process, thereby reducing the risk of errors while improving the efficiency of production cycles. What’s more, they are easy to use and maintain.
The solutions we offer are also tailored to the needs of laboratories and pharmaceutical production units. They enable isolators to be cleaned quickly between different production stages, without the need for complete sterilisation. This makes them a practical option for high-throughput facilities.
The CIP and WIP system in pharmaceutical isolators is therefore essential for maintaining the cleanliness and safety of pharmaceutical isolators. Thanks to its expertise and innovative solutions, EREA Pharma is a trusted partner for companies seeking to optimise their cleaning processes and benefit from sterile production conditions.
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