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Interflow has many Years of experience and has therefore become the clear leader in the specialist field of air control. On the basis of this specialism, Interflow has become a leading manufacturer of cleanrooms, operating theatres, steril preparation rooms and laminar flow units. From design to commissioning, we have all the experience in house to enable us to carry out the most diverse projects with the utmost precision and to the highest quality standard. Interflow is part of the BAM Techniek sector of koninklijke BAM Groep nv. Interflow is therefore, cepable to handle virtually every multidisciplinary project integrally regardless of its size and complexity.

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Specialist in clean enviroment

Interflow has many Years of experience and has therefore become the clear leader in the specialist field of air control. Interflow offers. On the basis of this specialism, Interflow has become a leading manufacturer of cleanrooms, operating theatres, steril preparation rooms and laminar flow units.

Clear Leader

Interflow has many years of experience and has therefore become the clear leader in the specialist field of air control. Interflow offers a total package, including training, support and maintainance. From design to commissioning, we have all the expertise in house to enable us to carry out the most diverse projects with the utmost precision and the highest quality standard. We can provide custom built solutions based precisely on our customer’s requirements for a specific process.

Integral implementation

Interflow has been part of BAM Techniek, a division of Royal BAM Group, since 2000. This enables us to implement virtually any project integrally, regardless of its size and complaxity. Our advisors, designers and specialist engineers in many disciplines ensure that every project is carried out efficiently and according to a tight project management plan. Large, multidisciplinary projects can also be carried out in conjunction with sister companies in Royal BAM Group.

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Product segments - Introduction

Customer focus from A to Z, that’s always been our goal. And not without succes. Interflow has grown to a modern, high-tech industrial company offering the following producsegments:

Cleanrooms

  • Cleanrooms for industries such as pharmaceuticals, microelectronics and medical equipment suppliers.

Operating Theatres

  • Operating theatres and sterile preperation and treatment rooms

Laminar flow

  • Microbiological safety cabinets
  • Crossflow units
  • Downflow units and fan filter modules
  • Isolators and mini-environments for production and sterility monitoring

Extraction units

  • Powder extraction units
  • Table top fume hoods

Vaildation and Measuring services

  • Provision of a wide range of validation and measuring services, including maintainance.

Our advisors

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Introduction Cleanroom Products

Cleanrooms: From necessity a must!

Cleanroom technology originated in the early 1960s. The battle to reach the moon first resulted in the development of advanced rockets. The available space was very limited in these rockets. This lead to the miniaturisation of electronic components. The previously negligible effect of microscopic dust and particles started to have a negative effect on electronic components due to this miniaturisation. It was decided that the amount and size of the dust and particles in the production area had to be limited. The idea was successfully realised and the concept of ‘Cleanrooms’ was born.

 

Cleanroom Classification

There are several standards for the classifications of Cleanrooms: The NEN-EN-ISO 14644- 1:1999 ‘Cleanrooms and Associated Controlled Environments, Part 1: Classification of air cleanliness’ issued in January 1999 is an international ISO standard. GMP is short for Good Manufacturing Practices.

 

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Humans as the Main Containment

A balance is obtained when the air mixture in a turbulently ventilated Cleanroom is ideal. This balance depends on the emission of particles in the room and the dust content or particle concentration in the supplied air. Interflow usually filters the air supply using High efficiency filters. This guarantees that the dust content or particle concentration in the air supply is controlled. The emission of particles in the room is indicative for what concerns the quantity of supplied air and the degree it can be made dust-free. The main dust producer in a Cleanroom is the human user.

 

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From Design to Validation

Interflow can help you decide which dust-free class you require. Many questions also need to be answered, such as, what the required temperature and relative humidity should be in the Cleanroom, what type of cooling system should be used, etc. Since you will not be dealing with these types of questions on a daily basis, we suggest you seek advice from our dedicated consultants. We, therefore, aim to provide a Cleanroom which is as cost-effective as possible and that is conspicuous due to its simplicity and reliability.

Operating Theatres

A complete system for operating theatres

Our extensive experience of designing, installing and building Cleanrooms enables Interflow to offer a full range of operating theatre systems. From idea to realisation Interflow is specialised in the design of complete operating theatre systems in line with your exact requirements. Interflow’s design remit is not just limited to the operating theatres themselves, but the totality of the OT-environment from sterile storage to recovery room settings. In this concept, the designer and the supplier are directly responsible for the end result. The Interflow OT-system guarantees that all components are installed in such a fashion that: contamination is kept to an absolute minimum during operations, pressure hierarchy and room classifications are guaranteed, finishings are sealed and optimal. As fully qualified contractor and part of BAM Techniek, Interflow has all the resources at its disposal to design and implement a complete system for your operating theatre complex. These include: engineering systems, including the air-conditioning system, electrical system, data and communication system and medical gasses.

 

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Laminar flow

Since the early 1970s Interflow has been working with researchers, doctors and ventilation engineers to develop groundbraking solutions of ‘laminar flow’ technic, which resultet in a large range of Laminar flow cabinets

Work method

Two aspects are indispensable when ensuring clean air: Laminar flow and Filtration.

  • Laminar flow is a very constant and unidirectional airflow which moves within a working area at a prescribed speed. This airflow transports all unwanted particles away from the critical area, be it the area around humans, the product or both
  • Filtration ensures that all unwanted contaminants - no matter what size - are removed from the air.

The right solution without exception!

Clean air is essential to many (production) processes and is not limited to operating theatres or the production of microelectronic elements. Interflow has an extensive range of units and cabinets to create the required protection. At our company, every solution is custom-made. Interflow ensures the meeting of your objective, that is, clean air by the square metre, in a professional and reliable manner.

 

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Safety extraction units

A pleasant and clean environment is a must in order to work pleasantly and efficiently. When this is combined with optimal safety and proven certainty, performance will reach high levels. Interflow combines all of the above elements in its safety exhaust units. All types of powders, gasses, vapours and aerosols, which are a health-risk for humans, are produced during industrial processing. When it is not enough to counteract these elements at the source, the second strategic step is to screen off this source using Safety exhaust units.

How...?

Interflow powder extraction units are extremely suitable to protect against hazardous powders that are released into the working area. Fume cupboards are especially suited to the extraction of gases and vapours. Interflow produces all types and sizes of fume cupboards. Interflow draws from an extensive ventilator range and a broad selection of filtration techniques when producing customer-specific solutions. Your breath of fresh air is in our care!

 

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Total Solution

Interflow does not deliver a do-it-yourself kit but the total solution. Consulting our customer every step of the way, Interflow is able to advice, develop, construct, install and validate the required solution. Together with our customers, we can guarantee a total solution. Not poor quality but top quality!

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Validation and Measuring

Optimal safety: a matter of life and death! You should always have confidence in your cleanroom, laminar flow equipment, microbiological safety cabinets and exhaust units. The production process and/or workers should not be in contact with hazardous substances. Should these be dust particles, microbiological contaminants or noxious gases and vapours.

 

Interflow is well aware of the possible dangers when an installation does not operate appropriately. All installations and equipment should periodically be checked thoroughly to keep these risks to an absolute minimum. The periodic inspection (validation) can be performed by Interflow’s independent Validation and Measuring department. This department provides the “documented verification which offers sufficient certitude that a specified process meets the pre-set specifications” (validation), required by various monitoring bodies, such as the FDA and GMP.

 

Interflow is able to take care for the validation of the next equipment, installations and environments:

  • Cleanrooms (As-built, At rest en Operational)
  • Operation theatres
  • Laboratories
  • Air conditions plants
  • Cross flow units
  • Down flow units
  • Microbiological safetycabinets
  • Insulators
  • Exhaust units and afzuigpoints
  • Fume cabinets
  • Powder extraction units
  • Overpressure units
  • Chemical storage cabinets
  • Monitoring-systems

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Our advisors

Gijs Hillen

 

Gijs Hillen

Cleanrooms

Phone +31 651381604

Peter Roskam

 

Peter Roskam

Laminar flow products

Phone +31 653541205

Ben Visser

 

Ben Visser

Validation- and Measuring

Phone +31 653704612

 

Peter Lamberts

Validation- and Measuring

Phone +31 653402755

 

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