Global Cleanroom Expertise: Capabilities

Global Cleanroom Expertise: Capabilities

As you may already know, the Angstrom Technology Group of market leading cleanroom companies in the US, UK, and Europe has capabilities to provide multinational services to our global clients. But what does this mean for our customers?

The stringent control of process variables is a global requirement for pharmaceutical, electronics, and biotech industries worldwide. Our cleanrooms support top-tier multinational organizations to increase quality at sites across the world.

 

EXPANDED PRODUCT RANGE

Through in-house expertize and collaborations with specialist industry-partners, we can deliver facilities with precise requirements, such as battery dry rooms or cell and gene therapy suites.

 

CONSISTENT QUALITY

When it comes to global operations, maintaining consistent quality standards is crucial. Angstrom Technology understands this well and no matter where you are in the world, we can deliver compliance to the applicable regulations. This commitment to quality gives you the reassurance that partnering with Angstrom Technology will result in reliable and high-performing solutions for your business.

 

FASTER RESPONSE TIMES

In a fast-paced business environment, time is of the essence. Angstrom Technology’s global network of partners enable us to reduce shipping and installation times significantly. This streamlined approach translates into improved operational efficiency for your business, giving you a competitive edge.

 

LOCALIZED SUPPORT CAPABILITIES

By having a network of support teams strategically located across different regions, Angstrom Technology ensures that you receive personalized attention and timely assistance. This localized approach strengthens our commitment to customer satisfaction and builds long-lasting partnerships.

 

COMPETITIVE PRICING

Angstrom Technology’s global capabilities enable them to optimize their supply chain and take advantage of economies of scale. This optimized approach allows them to offer competitive pricing without compromising on quality. By partnering with Angstrom Technology, you can access cost-effective contamination control.

 

ACCESS TO GLOBAL EXPERTIZE

With a multi-disciplined, in-house team of cleanroom experts, we have expansive industry experience, with applied knowledge and skills across the globe, such as our global regulatory governance team.

 

GLOBAL CLEANROOM PROJECTS

 

Capabilities - Global cleanroom customers

 

SPEAK WITH THE EXPERTS AT ANGSTROM TECHNOLOGY

If your facility needs a new cleanroom, Angstrom Technology can design, build, and install one that meets your specifications. Using proven design strategies and quality build systems, you can trust that your work and employees will always be protected.

Request a cleanroom quote today, or contact our team for more information.

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Global Cleanroom Expertise: Regulatory Governance Team

Global Cleanroom Expertise: Regulatory Governance Team

The regulatory landscape for cleanrooms can be complex. On top of managing the requirements of the ISO 14644 suite of standards, you may also need to comply with cGMP (Good Manufacturing Practice) guidelines and those of industry regulatory bodies. But the experts at Angstrom Technology are committed to supporting you through successful audits. All cleanroom projects with a requirement for cGMP compliance have oversight from our dedicated regulatory governance team. 

With over 40 year’s combined experience in cGMP and pharmaceutical industries, this level of in-house expertise sets us apart from other cleanroom companies. In this blog — the first in our Global Cleanroom Expertise series — we explain how we can support your regulatory compliance.  

 

Meet the Regulatory Governance Team

Global Compliance and Quality Assurance Manager

Global Compliance Lead

Joan Benson - Global Compliance and Quality Assurance ManagerSimon Rice - Global Compliance Lead
Joan has 30 years previous experience in Cell and Gene Therapy, Academia, Pharmaceutical Industry, Contract Clinical Research and Hospital Aseptic facilities. She was front facing regulatory inspections in MHRA, FDA, HTA and HFEA for 20 years.Simon has 8 years previous experience in the production of radiopharmaceuticals within a fully accredited GMP facility manufacturing sterile pharmaceuticals. This gives him a unique understanding on the implications of GMP.

 

Regulatory compliance services

Our cleanroom systems can be qualified to cGMP, and the required ISO classification. Not only that, but they can also meet any applicable international engineering and building standards and regulations. Our skilled and multi-faceted team can provide the following key services to support your compliance: 

  • Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) 
  • Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT) 
  • Validation 
  • Audits of facilities and Quality Management Systems 
  • Gap analysis 
  • Mock regulatory inspections 
  • Bespoke validation studies 

 

Regulatory governance successes

Our team has led high-profile global cleanroom projects to regulatory compliance. There are just a few of their recent successes. 

  • Led cleanroom validation (DQ, IQ, OQ, PQ, FAT, SAT and a wrap-around validation package covering EMS, VHP systems and cryostorage) for a 33-room Cell and Gene Therapy Manufacturing Facility. 
  • Led cleanroom validation (DQ, IQ, OQ, PQ, and all commissioning data) for a 6,500 Cleanroom Facility in their 11,000 square feet Single-Use Bioprocessing Technologies Manufacturing Facility. 
  • Supported numerous clients on the delivery of their projects with regulatory support on all aspects including design, validation, and commissioning 
  • Led cGMP qualification packages for current clients with GMP facilities 
  • Gap analysis for leading clinical research units 

 

Ready to start your cGMP cleanroom project? Contact us

We are committed to supporting you through successful audits and inspections, now and in the years to come. To learn more about our cGMP cleanroom design-build services, request a quote or contact us. 

 

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What are Semiconductor Cleanrooms?

What are Semiconductor Cleanrooms?

Semiconductor chips are used in every computerized device — from household objects like your cell phone or coffee maker to complex machines like vehicles, defense technology, or spacecraft. They’re produced using highly sensitive materials to create delicate layers that must be worked on with care. That’s why tasks like semiconductor chip manufacturing, testing, and packaging must be carried out in a controlled cleanroom environment.

Below, we explore more about semiconductor cleanrooms, including their common applications, classifications, and design features.

What are Semiconductor Cleanrooms?

Before we dive into the many specialized features of semiconductor cleanrooms, let’s back up and get a better understanding of what semiconductors are and why they must be handled within a cleanroom.

What Are Semiconductors?

Semiconductors are made using a glassy, solid material of pure silicon, which is shaped in a molten state and then cut into thin wafers. Semiconductors are prized for their special conductive behavior — which behaves both like a metal and an insulator — and are a vital ingredient for manufacturing computer chips and circuitry. A wafer is a substrate that’s used for the base in an integrated circuit, or chip.

Semiconductor chips are fragile materials. Even the slightest inconsistency can compromise their safety and effectiveness — and in turn, compromise the safety and effectiveness of the machines and equipment powered by those chips. That’s why semiconductor cleanrooms are important and why they must comply with strict standards to ensure total control over the chip manufacturing environment.

Boost to the Semiconductor Industry

In August 2022, the United States government passed the CHIPS and Science Act. This act was created with the intention to boost semiconductor chip manufacturing and bring more of it back to the U.S. rather than overseas. It authorized nearly $52 billion in government subsidies for U.S. semiconductor manufacturing and research, as well as an estimated $24 billion in investment tax credits for semiconductor chip manufacturers.

Needless to say, this act has impacted the nation’s semiconductor industry tenfold. Plants that once had to stall their semiconductor projects due to lack of funding and resources can now resume. Other semiconductor chip manufacturing companies are likely to expand their operations. In order to do that, they’ll need more cleanrooms.

 

Sound like you? Contact Angstrom Technology to get started on your semiconductor cleanroom project today. 

 

Semiconductor Cleanroom Applications

Semiconductors are used in many industries and applications. Whenever maintaining quality and purity in semiconductor chip manufacturing is crucial (which is all the time), a cleanroom is required. Some of the most common industries and applications that require semiconductor cleanrooms include:

Semiconductor Cleanroom Classifications

Semiconductor cleanrooms often run 24 hours per day due to our technologically inclined society’s demand for valuable circuitry components. Some of the most stringent cleanroom classifications must be maintained consistently throughout the chip manufacturing process.

In most cases, semiconductor cleanrooms must comply with ISO 14644-1 Class 4-6 requirements. This stipulates a maximum allowed particle count between 352-35,200 particles 0.5μm or smaller. They must also meet the requirements of ISO 14644-2, which imposes a quality control system in order to maintain these standards. However, not all processes require such stringent control. The packaging, assembly, and testing of manufactured wafers could be performed in ISO class 7 or ISO class 8 cleanrooms.

Depending on their unique application, semiconductor cleanrooms will also likely have to meet some industry-specific requirements, for example, ASTM standards for automotive applications and NASA standards for aerospace applications. These are usually complied with in addition to ISO standards to ensure that semiconductor cleanrooms are always controlled and that the chips that come out of them are of consistent quality.

Any drop below these stringent standards could lead to defects.

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Semiconductor Cleanroom Design

Semiconductor cleanrooms require a robust cleanroom design that helps them reach and maintain strict cleanliness standards while also allowing for easy movement and workflow. Here are a few especially important semiconductor cleanroom design aspects to consider.

Operators & Operator Processes

Just like with any other type of cleanroom, the biggest threat to cleanliness and control in semiconductor cleanrooms is the people working within them. That’s why semiconductor cleanroom operators must be specially trained and outfitted to prevent contamination.

But this semiconductor-operator relationship goes both ways. Semiconductors and the processes that are needed to manufacture circuitry from them can be harmful to human health. Therefore, it’s important to design semiconductor cleanrooms in way that allows operators to complete tasks safely. Some semiconductor cleanrooms even have robotic equipment or special safety protocols in place to protect workers from radioactive processes, toxic chemical exposure, lasers, and magnetic fields.

Air Quality & Filtration

As mentioned above, semiconductor cleanrooms must have a high level of air quality — some of the cleanest air required for any cleanroom application. This starts with powerful cleanroom HVAC and filtration systems, like HEPA or ULPA filters, which are used to process the air to remove particles up to allowed limits.

Machines within the cleanroom may also have their own exhaust system that removes unclear air and particulate matter.

Other Environmental Threats

Aside from airborne particle filtering, semiconductor cleanrooms must also be protected against other environmental threats. Control is especially important over factors like:

  • StaticElectro-static discharge damages the conductive properties of semiconductors. Static dissipative materials for flooring, wall panels, furniture, and more must be used.
  • Humidity – Uncontrolled humidity in semiconductor cleanrooms can result in inconsistent bake-out times, surface swelling and corrosion, and evaporation of solvents. A consistent relative humidity between 35-65% is necessary.
  • Out-gassing – Semiconductor cleanroom equipment can produce outgassing and introduce airborne contaminants into the space. This must be controlled with proper equipment cleaning and maintenance, as well as consistent air filtration.

Do You Have a Semiconductor Cleanroom Project in Mind? Let’s Talk!

If your facility needs a new semiconductor cleanroom, Angstrom Technology can design, build, and install one that meets your specifications. Using proven design strategies and static dissipative materials, you can trust that your work and employees will always be protected.

Request a semiconductor cleanroom quote today, or contact our team for more information.

Whitepaper: Dry room design guide for lithium battery manufacturing

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Cleanroom Construction in your Existing Structure

Cleanroom Construction in your Existing Structure

Constructing a cleanroom in any space is a major advantage of the modular cleanroom building process. Let’s look at where you can build a cleanroom in your current space and what that process looks like.

WHERE CAN YOU CONSTRUCT A CLEANROOM?

Retrofit cleanrooms can achieve any ISO cleanroom classification, and construction can happen in various spaces. However, the best type of cleanroom for each space may differ. Let’s take a look at three examples.

1.     CLEANROOM CONSTRUCTION IN A LARGE INDUSTRIAL SPACE

If you’d like to construct a cleanroom in a large space such as a warehouse, you have a lot of freedom when it comes to the square footage and layout of your cleanroom. Although you have plenty of space, it’s important only to build the cleanroom as large as it needs to be. This will not only save you money on materials during cleanroom construction but will also cut down energy usage once the cleanroom is in operation.

In a large space, you can suspend modular cleanroom panels from a strong ceiling grid or build a freestanding cleanroom. Your cleanroom can also be constructed to include existing walls, utilize light from existing windows, and even connect to the utilities of the building — as long as they meet your cleanroom classification requirements. Any type of modular cleanroom is suitable for a large space, so you can choose between a HardWall, SoftWall, RigidWall, or Seamless cleanroom — whatever will be best for your application.

2.     CLEANROOM CONSTRUCTION IN SMALL SPACES

Although large spaces offer plenty of room to spread out, don’t discount smaller spaces for cleanroom construction. A flexible modular cleanroom type — such as SoftWall cleanrooms — can be highly effective in a tighter space. SoftWall modular cleanroom panels can be arranged into more condensed layouts than their HardWall or RigidWall counterparts while still achieving ISO Classes 4-8.

Additionally, the modular design means SoftWall cleanrooms can be set up quickly, easily reconfigured or taken down and stored, and moved virtually anywhere you need a cleanroom.

3.     OFFICE SPACE TO CLEANROOM CONVERSION

Unused office space presents a great opportunity when looking for space to install a new cleanroom. A new cleanroom design can incorporate many elements of the existing structure. Depending on your cleanroom’s requirements, you may be able to use an existing ceiling grid, walls, and windows.

To convert office space into a cleanroom, you must upgrade each surface to create a flush, non-particle-shedding structure. HardWall cleanroom walls are ideal for office space conversions — offering a high level of control over environmental conditions within the space. The retrofit cleanroom design might also include antistatic flooring, a grid lighting system, and an airflow pattern that works with the customized space.

 

RETROFIT CLEANROOM CONSTRUCTION PROCESS

The process of retrofit cleanroom construction in every space will look a bit different, as it’s highly customized to each application. It involves four main steps, of which the first two are the most critical. Those include site survey, design, construction, and installation.

1.     CLEANROOM SITE SURVEY

Cleanroom construction in an existing structure relies on the planning stages to ensure your space can support the cleanroom you need. Before any work begins, a cleanroom expert must assess the space to determine whether it will accommodate the necessary equipment, furniture, and personnel. They’ll also examine the quality of the room’s air to specify filtration needs and determine what systems can be adapted or replaced.

2.     CLEANROOM DESIGN

When designing your retrofit cleanroom layout, the cleanroom designer will need to factor in how the space influences the airflow pattern. A cleanroom design expert uses computational fluid dynamics to map out the airflow pattern for your application and layout. They’ll need to know where furniture and equipment will be installed to optimize the design.

3.     CLEANROOM CONSTRUCTION

With the design complete, it’s time to move on to cleanroom construction. With modular cleanrooms, the structure is built to meet the design specification and the cleanroom’s classification standards. They are pre-wired and pre-insulated so they can be quickly assembled and installed in the existing building once they arrive.

4.     CLEANROOM INSTALLATION

Finally, the cleanroom is ready for installation in your existing structure. The installation process will be straightforward after spending more time planning and designing the cleanroom to work in your space. Modular panels will be attached to existing walls, and new walls will be set up to be either freestanding or suspended. An installation team will install HEPA filters lighting systems in the ceiling, then connect the cleanroom HVAC system.

Cleanroom construction in an existing structure requires extra care and attention. Due to the cleanroom’s critical nature, we recommend having a team of experts install the cleanroom into your space to ensure a flawless end product. This way, you get a suitable cleanroom for your application and space.

 

SPEAK TO THE EXPERTS AT ANGSTROM TECHNOLOGY ABOUT YOUR RETROFIT CLEANROOM

Are you wondering if you can build a cleanroom in your space? Give Angstrom Technology a call! Our professional cleanroom designers can assess your site and design a cleanroom that will work perfectly in your space. To get started, give us a call or reach out to us online today.

 

 

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Angstrom Technology Appoints Tom Chowaniec as New Global CEO

Angstrom Technology Appoints Tom Chowaniec as New Global CEO

PRESS RELEASE

Angstrom Technology, a global cleanroom engineering company and portfolio company of ASGARD Partners & Co., welcomed Tom Chowaniec as its new Global CEO.

Chowaniec comes to Angstrom Technology with over 30 years of professional experience leading global sales and service teams at GE Healthcare, Cardinal Health, Leica Microsystems and Agiliti Health. He has an accomplished track record of satisfying customers, creating career opportunities for employees and acquiring and integrating new businesses. Tom received his MBA with Honors at The University of Chicago in 1998. He also received a bachelor’s degree in electrical engineering, magna cum laude, from Marquette University in 1993.

“We are excited to welcome Tom to our global group of cleanroom companies,” said Matt Isard, CEO of Angstrom Technology. “We believe he is the ideal Global CEO to lead Angstrom’s next chapter of growth and success, as we continue to expand our portfolio in the cleanroom market through global acquisitions.”

Tom succeeds Isard as Global CEO, heading up the company’s four locations:

  • Grand Rapids, Michigan
  • Lancaster, U.K.
  • Wycombe, U.K.
  • York, U.K.

Isard will stay with the company as CEO and continue to hold his seat on its board of directors.

About Angstrom Technology

Founded in 1989 and headquartered in Grand Rapids, Michigan, Angstrom Technology offers design, engineering, and build capabilities to the cleanroom industry. As a market leader in cleanroom production across North America and Western Europe, Angstrom serves clients in industries like aerospace, defense, technology, pharmaceutical, automotive, gene therapy, medical packaging, medical device and more. Angstrom’s passion is to provide its customers with the most effective and efficient designs, superior quality and outstanding service. For more information about our market-leading cleanrooms or to start a project with us, please contact us.

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