UKAS calibration accreditation for PMT (GB) Ltd

Published: 20-Sep-2010
Design & Build Analysis

First accreditation of its kind to be awarded for particle counter calibrations in the UK


PMT (GB) has achieved UKAS Accreditation for the calibration of particle counters at its Malvern-based laboratory.

The company is accredited in accordance with the recognised international standard ISO/IEC 17025:2005 for the General Requirements for the Competence of Testing and Calibration Laboratories.

This is the first accreditation of its kind to be awarded for particle counter calibrations in the UK.

“It has been a tough and long process to achieve this accreditation,” said Ian Norman, PMT (GB)’s Customer Service Manager, “but our whole team has worked very hard to satisfy the requirements of UKAS.”

Clients who use PMT (GB) can now have an even greater confidence in the competence and quality of the service provided.

Please have a look at: www.particle-accreditation.com.

  • Companies:
  • PMT GB
See more

You may also like

Analysis

New active air sampler on the market is Annex 1-ready

Read more
The equipment has been designed to meet the latest standards for continuous viable monitoring

Trending Articles

  1. AAF inaugurates new cleanroom facility for HEPA filter manufacturing Designed to meet customer requirements for clean manufacturing and product quality
  2. 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
  3. Integrity testing of HEPA filters: A practical approach Filtering the air in aseptic process areas is critical to maintaining the cleanliness of the production environment. Jesus Casas provides tips to ensure HEPA filters are fit for purpose once installed in your facility
  4. Bonalive Biomaterials expands production capabilities The medical technology company has moved its headquarters to a new building with increased production capabilities. The construction and renovation of the new building is in the cleanroom validation stage
  5. How-to guide: Pass box qualification Material transfer equipment plays an important role in minimising contamination risks during the manufacturing process. Industry expert, Jesus Casas, gives an overview of available pass boxes and a step-by-step explanation on how to qualify them appropriately

Upcoming event

Pharmig Annual Pharmaceutical Microbiology Conference

20–21 November 2024 | Conference | Nottingham, UK See all

You may also like

Analysis

New active air sampler on the market is Annex 1-ready

The equipment has been designed to meet the latest standards for continuous viable monitoring
Analysis

Compact FMSnode integrates cleanroom sensors

It has an open software structure and modular design
Design & Build

Counting airborne bacteria in real time

Measuring system does away with the need for costly sample preparation
Design & Build

Selecting an airborne-particle counter for your environment

Understanding which features you need in a particle counter is a difficult task. This article will identify the various features available and help you choose which are relevant to your application
Design & Build

Particle monitoring requirements in pharmaceutical cleanrooms

GMP regulations require that these environments are rigorously monitored to ensure that there is full and constant awareness of current environmental conditions, both for viable and non-viable contamination
Design & Build

Particle monitoring in high-pressure gas lines

In today’s high-tech manufacturing processes, there are a diverse number of procedures demanding minimal levels of particle contamination. With continuous monitoring improvements, the minimum thresholds are always being challenged for an environment to become “more clean”.
Design & Build

GMP particle sensor – data security guaranteed

Integrated data logger backs up eight hours of particle data
Subscribe now