Our customers can be confident that ATS has the world-class processes in place to meet even the strictest quality standards


ATS has been registered to the ISO 9000 generation of standards for over 20 years. A central component of the ATS quality management system is based on the PDCA model

ATS maintains a global registration to ISO 9001 and has expanded to ISO 13485 and ISO 27001 for several key divisions. In addition, ATS has incorporated a quality management system compliant to NQA-1, 10 CFR 50 Appendix B, 10 CFR 21, CSA N299.1, CSA N286, CSA N285 & CSA B51 with in the Nuclear division.

Licenses and Registrations


GMPs are the guidance’s arising from various regulatory bodies’ legislations. They form the foundation for the practices and systems to be adhered to in manufacturing, quality control, and distribution of life sciences related products. They cover the manufacturing, testing, and packaging of pharmaceuticals (including active pharmaceutical ingredients), diagnostics, foods, medical devices, combination products, blood and blood components, and biologicals. The intent of the GMPs is to ensure patient safety through product integrity.

ATS applies Good Manufacturing Practices (GMP) to life sciences and nuclear programs through machine design, materials-for-construction selection, assembly methods, documentation, change control and validation.

Note: Applicable to certain divisions


Global Director, Mission Assurance & Compliance

Please contact the Global Director, Mission Assurance & Compliance for more information on ATS’ quality foundation and associated programs.

Global Quality System Manual

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Licenses and Registrations

View ATS Licenses and Registrations
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