An overview of USP <1660> testing strategies for glass pharmaceutical container performance

Making informed packaging decisions requires a clear understanding of how container materials behave over time when in contact with pharmaceutical products. This guide outlines proven analytical approaches for evaluating container performance, identifying potential quality concerns, and monitoring changes that may affect product stability.

Readers will learn how predictive studies and specialized testing methods can help support regulatory expectations, optimize packaging selection, and reduce product development risks.

Whether involved in quality, analytical testing, packaging, or regulatory affairs, professionals will gain actionable knowledge to support safer and more reliable pharmaceutical products. 

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Glass vials on a production line representing pharmaceutical testing in Intertek Pharmaceutical Services India laboratory

Intertek Pharmaceutical Services India

Analytical Testing, Auditing and Process & Powder Safety Testing US FDA, MH-FDA, CDSCO, cGMP, GLP & NABL Certified Laboratory


Intertek Pharmceutical Services India
F-Wing, Tex Center, Chandivali Farm Road,
Chandivali, Andheri (E) Mumbai,
Maharashtra - 400072
T: +91 1246 703703
T: +91-22-4245 0100
E: pharma-asia@intertek.com


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