Agilent's Quality Policy is to earn customer loyalty by providing products, services, and interaction experiences of the highest quality and greatest value. One way in which they are implementing this policy is through their commitment to maintaining product and service Business Management Systems to conform to the requirements of ISO 9001:2008 and/or ISO 13485:2003 (the medical device standard) as appropriate for specific markets.

Agilent’s product development, manufacturing and service/support operations meet applicable ISO requirements and most are certified to the ISO 9001:2008 standard. In achieving ISO 9001:2008 or ISO 13485:2003 certification, Agilent has demonstrated to third-party auditors that they have certain processes in place and under control. These processes involve activities as listed below. Additionally, Agilent maintains a company-wide ISO 14001:2004 certificate for their Environmental Management System.

  • Calibration
  • Continuous process improvement
  • Corrective action
  • Customer satisfaction
  • Document and record control
  • Incoming quality control/In-process inspection/Final inspection
  • Internal audits
  • Inventory management
  • Management review/Management involvement/Resource management
  • Procurement control
  • Statistical process control
  • Training/Certification
  • Organisation structure/Organisation change

Do you need an ISO Certificate?

If you require a copy of an ISO certificate related to a particular Agilent product, please visit the Agilent Quality Policy & Resources web page by clicking on the button alongside.

Based in the heart of Newcastle University campus, HistoCyte Laboratories Ltd is certified to the EN ISO 13485:2016 standard. They have been able to work closely with academic scientists and pathologists in order to test their product range and engage with experts in the histopathology field.

This, together with the relationships they have developed with other key opinion leaders and institutions, has allowed them to clearly identify the needs of scientists. As a result, they aim to deliver high quality, reproducible and cost-effective analyte control material for same-slide use in histopathology

Do you need an ISO Certificate?

If you require a copy of the HistoCyte Laboratories ISO certificate click on the button alongside.

Lucigen’s quality system is registered to the ISO 13485:2003 international standard for the design, manufacture, and distribution of medical devices. This standard describes the requirements for developing, producing, distributing, and maintaining high quality products and services for scientists working in the medical and life sciences. Their quality management system certification to the ISO 13485:2003 standard by British Standards Institute (BSI, Inc) assures customers that Lucigen has a compliant and effective system in place to deliver the highest quality products that clients expect.

Lucigen has adopted a process-based quality management system as the way they accomplish daily work and deliver the products you require when you need them. Process-based quality starts with the principle that the customer is the final judge of any company’s value. Lucigen’s work is organised to understand what customers require, to design the most reliable way to produce and deliver it, and to measure how they are doing every step of the way.

Do you need an ISO Certificate?

If you require a copy of the Lucigen ISO certificate click on the button alongside.