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  • Global quality systems 


    Quality is the basis for everything we do at Avantor®, and our commitment to patient welfare is reflected in our proven global quality systems.

    We offer application-specific consistency and trace element characterization to match customer requirements as closely as possible. This helps streamline product development and can directly impact process productivity and drug safety.

    Global cGMP manufacturing

    Avantor offers cGMP manufacturing facilities in  Avantor's cGMP manufacturing facilities in the U.S., Europe and India.

    Secure and reliable global supply chain

    From the acquisition of raw materials through production and shipping, we emphasize quality and security in both our own operations and those of our suppliers, and we track and share how we're doing with our customers.

    Management of change

    Our Management of Change control notification allows customers to understand exactly what changes are happening, what products are affected and how far-reaching the impact could be.

    ISO 9001-compliant quality management systems

    All of our manufacturing facilities are ISO 9001:2008 certified, and we use MasterControl™ as our global electronic quality system to document. 

    Continuous improvement

    Our quality systems drive continuous improvement across our production and distribution systems.

    Innovative packaging options

    Avantor offers fully integrated, state-of-the-art delivery platforms and custom solutions at any scale. Regulated and highly regulated grades of Avantor products also feature tamper-evident branded seals on outer packaging.

    GHS labels and SDS

    All of Avantor's U.S. product labels and safety data sheets are GHS compliant.

    Multicompendial product standards

    Avantor offers a comprehensive range of multicompendial products including USP/NF/FCC, EU, JP, and IP. This allows us to meet the needs of pharmaceutical customers around the world.

    Globally accepted documentation support

    Avantor shares full regulatory data regarding pharmaceutical production chemicals so you can file your drug applications with global regulatory authorities. For certain excipients that are classified as APIs, we provide FDA-reviewed Drug Master File documentation, as well as expertise and help in completing documentation.

    Manufacturer batch tracking (parent lot)

    Manufacturer batch tracking allows customers to identify the origin of raw materials repackaged by Avantor, providing greater traceability of materials.