Compliance & Certification
Avantor is fully committed to complying with the regulatory requirements in every region in which we operate.
Our Regulatory Affairs Department has expertise in a wide array of regulatory domains relevant to the life sciences industry. They routinely interact with regulatory organizations and authorities throughout the world and ensure Avantor has the right to conduct business involving regulated products, thereby supporting a reliable supply chain that can be trusted by our customers and others.
We have filed and maintain close to 800 master access files (“MAF”) and drug master files (“DMF”) that are registered with regulatory authorities globally— helping to simplify medical and pharmaceutical product approval processes by allowing manufacturers to reference our products as part of their own applications.
ISO Certifications
Our management systems, manufacturing processes, services and documentation procedures are designed to fulfill the requirements of our various certifications and regulatory approvals. Our Global Quality Management System is scalable to create a consistent customer experience in the different markets we operate.
We are proud to hold current certifications in the following ISO Standards:
- Quality: ISO 9001 and ISO 13485 and other certifications
- Environment: ISO 14001
- Health & Safety: ISO 45001
Read our full list of Quality Management System Certifications helping us meet and exceed customer expectations.
Read our full list of other local certifications helping us meet and exceed environmental and health and safety expectations.