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Featured companies in Regulatory

FMS (Facility Monitoring Systems Limited)

FMS (Facility Monitoring Systems Ltd) provides airborne particle counters, Environmental Monitoring (EM) systems, Far-UVC decontamination solutions, contamination control...

MSL Solution Providers

MSL Solution Providers (MSL) is a microbiological testing laboratory, specialising in efficacy testing of biocides and disinfectant products used in a wide range of...

Lighthouse Worldwide Solutions

Lighthouse offers the most complete line of contamination monitoring solutions.

Air Techniques International

The leading designer and manufacturer of specialized test equipment for HEPA filters, flat sheet media, filter cartridges and respirators..

Wickham Micro

Microbiology testing with over 60 years of experience in medical device testing and pharmaceutical testing

PBSC

35 Years of Excellence - Established in 1987, PBSC has become one of the leading manufacturers of Clean Room, High Containment and Material Decontamination products throughout...

STERIS Life Sciences

STERIS Life Sciences is a global leader in contamination control for pharmaceutical manufacturing, biotechnology, research and laboratory settings. Our expertise is rooted in...

Charles River Microbial Solutions

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guides us in...

Crowthorne Group

Crowthorne Group is the largest independent supplier of clean air and containment services to the UK and Ireland, and fast becoming one of the largest in Europe

Trending Articles

  1. Micronclean strengthens leadership with two internal promotions Appointments reflect commitment to internal growth and operational excellence
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    What is ISO 8 cleanroom classification? Each cleanroom class is denoted by a maximum concentration of particles per cubic meter or cubic foot of air. ISO 8 is the second lowest cleanroom classification
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    A question of quality: Implementing quality by design principles Jason Rossi from AST discusses how a systematic approach, “Quality by Design”, is used to design and develop of drug product manufacturing environment that prioritises...
  4. Understanding the difference between cleanroom qualification and validation Each serves a different purpose in ensuring your controlled environment performs as required, and both are vital in meeting compliance expectations
  5. Cleanrooms: What is the difference between clean-up period and recovery time? The implementation of the new Annex 1, and references to the ISO 14644 family of cleanroom standards have raised questions around the "Recovery time" and the "Clean-up period."...

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Design & Build Each serves a different purpose in ensuring your controlled environment performs as required, and both are vital in meeting compliance expectations

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A question of quality: Implementing quality by design principles

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Sustainability Purolite AP+50 supports cost-efficient, high-performance bioprocessing at scale

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Design & Build Controlled environments are supporting quality, safety and regulatory compliance in cannabis manufacturing

Medicinal cannabis production with GMP-compliant cleanroom solutions

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Design & Build The laboratory services provider has started a major expansion of sterility assurance facilities to meet rising global demand and stringent EU GMP Annex 1 standards

Nelson Labs to double cleanroom capacity at US headquarters

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Sustainability Fluid transfer solutions company recognised among top 1% of global performers

NewAge Inc. awarded platinum EcoVadis rating for sustainability

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Containment Explore how a modern microbial method can improve contamination control and data quality

Uncovering blind spots in environmental monitoring

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Regulatory Peter Thistlethwaite from MSL Solution Providers explores the role of biocide regulations in maintaining the safety of cleanroom environments

The role of biocide compliance in cleanrooms

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Regulatory The 2023 revision of Annex 1 has left Part IV outdated, missing key references to QRM, CCS, modern technologies, and barrier systems

EMA proposes revision to GMP guidelines for ATMP production

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Design & Build A robust contamination control strategy begins with GMP-compliant design, hygienic construction and proper maintenance

Cleanrooms and clean utilities: The importance of sound design and construction

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Design & Build The Guardtech Group’s heritage turnkey brand are utilising state-of-the-art software to take their offering to another level

Cleanroom Solutions embracing the future to elevate their large-scale facility construction provision

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Regulatory With growing global demand for advanced diabetes treatments, an insulin manufacturer has partnered with Austar to strengthen its regulatory compliance and accelerate...

Austar delivers compliance consulting for major high-tech insulin manufacturer

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Design & Build The US President has signed an executive order to direct the FDA to review current regulatory procedures, such as by reducing inspection frequency

President Trump signs order for “regulatory relief” for domestic pharmaceutical manufacturers

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HVAC EN 16798-3 standard sets new air filtration requirements for non-residential buildings, aligning with the World Health Organisation air quality guidelines

Camfil welcomes updated EN 16798-3 air filtration standard

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