Compliance & Certification
Our company is certified in several ISO Standards related to Quality, Environment, as well as Health & Safety.
These certifications are part of our commitment to excellence and continuous improvement in quality. They are the foundation for the value we deliver to our customers through every process, program, product and solution we offer. This ensures our management systems, manufacturing processes, services, and documented procedures meet all requirements for global standardization and quality assurance.
Please visit avantorsciences.com for a full list of all Quality Management System ISO certificates.
ISO 9001 certification is based on quality management system principles which includes strong customer focus, involvement of top management, standardized approaches and a continual improvement process. This standard is the global standard for quality management systems, ensuring that customers consistently receive quality products and services.
ISO 45001:2018 specifies requirements for an occupational health and safety (OH&S) management system, and gives guidance for its use, to enable organizations to provide safe and healthy workplaces by preventing work-related injury and ill health, as well as by proactively improving its OH&S performance. Our sites in many countries use this standard as a backbone to support a safe and healthy work environment.
ISO 14001:2015 specifies the requirements for an environmental management system that an organization can use to enhance its environmental performance. ISO 14001:2015 is intended for use by an organization seeking to manage its environmental responsibilities in a systematic manner that contributes to the environmental pillar of sustainability.
Our company has many initiatives around the world to manage its environmental responsibilities: Examples would be the reduction and recycling of waste or the reduction of water, fuel and energy consumption.
The ISO 13485 standard specifies the requirements for a comprehensive quality management system for the entire life-cycle, a.o. production, sales and supply, of medical devices and in vitro diagnostics.
ISO/IEC 17025:2017 specifies the general requirements for the competence, impartiality and consistent operation of testing and calibration laboratories.
ISO 17034:2016 specifies general requirements for the competence and consistent operation of reference material producers. It is intended to be used as part of the general quality assurance procedures of the reference material producer.
Please find a list of ISO certificates and contact details for your country below.
If you do have any further questions regarding our Quality Policy, please feel free to contact: