Displaying 1–25 of 35 results for Containment & Cleanrooms
How the use of aseptic split butterfly valve technology can prevent contamination
Revised GMP guidelines will strengthen emphasis on contamination control, impacting cleanroom performance qualifications
How the pharma industry's big ideas are impacting sterile manufacturing
Whatever their intended purpose, setting up a cleanroom requires careful consideration both in the design phase, and then in how you use it.
From minor updates to high-tech changes, vendors are helping pharma meet strict cleanroom standards
Thinking differently about material selection and system integration for biologics
How new fluid control technology is keeping drug innovation in motion
Big ideas are meeting the challenge of manufacturing in a tighter space
A comparison of several sterile processing techniques, including aseptic isolators, restricted access barrier systems and aseptic Split Butterfly Valve technology
Pharma’s All-Star tech lineup shatters records with plenty of hits.
Pharma’s leaders continue to pursue success through a strategy of careful capital expenditure investment with an eye on increased capacity, speed and efficiency in their facilities.
Every cleanroom requires a carefully controlled environment maintained with Good Manufacturing Practices to prevent contamination
Pharma’s top CMOs are playing to their strengths, toning operations and flexing their technical muscles in an effort to compete
AdvantaPass combines single-use tubing, connectors and seals with permanent, wall-mounted stainless steel components to eliminate cleaning validations associated with clean room protocols.
Denso created the VS-050 aseptic robot because of rapidly increasing demand in the pharmaceutical, medical and life sciences sectors. Now our customers in those areas with sterilization requirements can benefit from the high speed and other outstanding features of the VS Series.
Humans invading your sterile processes? Advances in aseptic processing technologies aim to keep their risk and contamination at bay.
Manufacturing HP active pharmaceutical ingredient drugs is a challenge best met with a thorough assessment of risk and a robust containment strategy
Testing reveals steam sterilization delivers packaging process performance improvements
Pepperl+Fuchs’ Aseptic Operator Interface Terminal offers a compelling value prop for biopharma production environments
This report explains how a wall pass-through system that incorporates single-use components can reduce contamination risks and the use of valuable resources.
Surrogate testing offers a way to provide meaningful performance information prior to dust collection system installation
G-Con's cleanroom PODS speed construction and commissioning of the Defense Advanced Research Projects Agency’s scalable vaccine facilities
Emerging trends in pharmaceutical manufacturing processes will spur innovation, competitive vitality and safety
Success depends on speed, and addressing all potential risks and regulatory questions from the earliest design stages.
An assortment of pump and valve innovations help provide clean process efficiencies.