Containment & Cleanrooms

Cleanrooms are the enclosed, classified spaces used for processing bio/pharmaceuticals in a contained space with controlled reduction of airborne particulates, including microbes. Virtually every facility producing biologics or pharmaceuticals has at least one cleanroom. Here you will find information about cleanroom design, construction, operation and regulations.

Articles

Pm2304 Hero 854x480 Operations
Pm2304 Hero 854x480 Operations
Pm2304 Hero 854x480 Operations
Pm2304 Hero 854x480 Operations
Pm2304 Hero 854x480 Operations

Beating the space crunch

The pharma industry is running out of lab and manufacturing space — but there are options
Shutterstock 1899127090
Shutterstock 1899127090
Shutterstock 1899127090
Shutterstock 1899127090
Shutterstock 1899127090

Modern pharma cleanrooms

With regulators revising policies to provide clarity around best practices for aseptic manufacturing, cleanrooms are evolving
Egnineering-Nov
Egnineering-Nov
Egnineering-Nov
Egnineering-Nov
Egnineering-Nov

Engineering Angles: Optimizing the facility design phase

Early planning will ensure pharma facilities meet requirements
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doctorhands2
doctorhands2
doctorhands2
doctorhands2

Keepin’ it clean in pharma

Raising the importance of hygiene in accelerated vaccine manufacturing
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Glove-Port-CRL-198
Glove-Port-CRL-198
Glove-Port-CRL-198
Glove-Port-CRL-198

Maintaining sterility in aseptic processing

Rapid Transfer Systems have become a popular method of transferring items in an era where containment systems are needed more than ever

Staying on top of contamination

Actionable strategies for efficiently and effectively detecting contaminates in pharma manufacturing
ondemand-cleanroom
ondemand-cleanroom
ondemand-cleanroom
ondemand-cleanroom
ondemand-cleanroom

Engineering Angles: DIY or CDMO?

Pharma entrepreneurs often have to choose between building their own facilities or outsourcing discoveries — but could there be a middle ground?
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Screen-Shot-2020-06-25-at-12.14.08-PM
Screen-Shot-2020-06-25-at-12.14.08-PM
Screen-Shot-2020-06-25-at-12.14.08-PM
Screen-Shot-2020-06-25-at-12.14.08-PM

Integrating BSCs into cGMP environments

Electronic monitoring of biological safety cabinets supports aseptic processes and cGMP compliance

Engineering Angles: Innovating cleanroom design

Cleanroom infrastructures must evolve to support the facilities of the future
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Screen-Shot-2019-12-13-at-3.16.02-PM
Screen-Shot-2019-12-13-at-3.16.02-PM
Screen-Shot-2019-12-13-at-3.16.02-PM
Screen-Shot-2019-12-13-at-3.16.02-PM

Compressed air quality

Particle analysis methods and ISO 8573 Standard updates
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ChargePoint-AseptiSafe-Bio-8-with-verifi-screen2-
ChargePoint-AseptiSafe-Bio-8-with-verifi-screen2-
ChargePoint-AseptiSafe-Bio-8-with-verifi-screen2-
ChargePoint-AseptiSafe-Bio-8-with-verifi-screen2-

Product Focus: Keepin' it clean

Innovations that make life easier in the cleanroom
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next-gen-cleanrooms-main
next-gen-cleanrooms-main
next-gen-cleanrooms-main
next-gen-cleanrooms-main

The next decade of cleanrooms

Pre-fab and modular cleanrooms are on the rise, but stick-built still dominate.
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figure3chargepoint
figure3chargepoint
figure3chargepoint
figure3chargepoint

Safe & sterile powder transfer

How the use of aseptic split butterfly valve technology can prevent contamination
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Screen-Shot-2019-08-12-at-2.46.25-PM
Screen-Shot-2019-08-12-at-2.46.25-PM
Screen-Shot-2019-08-12-at-2.46.25-PM
Screen-Shot-2019-08-12-at-2.46.25-PM

Qualifying your cleanroom

Revised GMP guidelines will strengthen emphasis on contamination control, impacting cleanroom performance qualifications
Fedegari-multi-process-and-robotics
Fedegari-multi-process-and-robotics
Fedegari-multi-process-and-robotics
Fedegari-multi-process-and-robotics
Fedegari-multi-process-and-robotics

Product Focus: Advancing aseptic processing

How the pharma industry's big ideas are impacting sterile manufacturing