- Testing Types
- USP ⟨660⟩ Containers – Glass Testing
Terms and Conditions
Sample Submission Form
Overview
USP ⟨660⟩ establishes the testing requirements for evaluating the hydrolytic resistance and chemical durability of glass containers used in pharmaceutical packaging. PLS Analytical performs USP ⟨660⟩ studies to help manufacturers assess whether glass packaging provides the chemical stability and protection required for its intended pharmaceutical application.
PLS Analytical performs USP ⟨660⟩ testing to evaluate the hydrolytic resistance of pharmaceutical glass containers using standardized analytical procedures. These studies assess the interaction between glass surfaces and test solutions to determine chemical durability, supporting packaging qualification, supplier evaluation, material selection, stability programs, and regulatory submissions.
Glass packaging must maintain its chemical integrity throughout a product’s shelf life to minimize the risk of product-container interactions, particulate formation, pH shifts, and other quality concerns. Evaluating container durability early helps manufacturers make informed packaging decisions and reduce development and regulatory risks.
PLS Analytical delivers USP ⟨660⟩ testing aligned with compendial requirements, helping manufacturers generate scientifically defensible data for packaging qualification, stability programs, and regulatory submissions.
Testing Services
PLS Analytical performs USP ⟨660⟩ testing to support packaging qualification, supplier approval, regulatory submissions, stability programs, and lifecycle quality management activities.
Hydrolytic Resistance Testing
Hydrolytic Resistance Testing
Hydrolytic resistance testing evaluates the chemical durability of pharmaceutical glass containers under controlled laboratory conditions. Scientifically robust data supports glass container qualification, injectable packaging systems, material performance assessments, and regulatory submissions.
Glass Container Characterization
Glass Container Characterization
Glass container characterization evaluates the critical properties that influence the suitability and performance of pharmaceutical glass packaging. Scientifically robust data supports packaging qualification, supplier evaluation, packaging change control, and material quality assessments.
Packaging Compatibility & Stability Support
Packaging Compatibility & Stability Support
Packaging compatibility and stability support evaluates the suitability of glass packaging systems for their intended pharmaceutical application. Scientifically robust data supports product-container compatibility assessments, stability studies, packaging qualification, lifecycle management, and regulatory submissions.
Advantages
USP ⟨660⟩ testing provides the scientific data needed to evaluate glass packaging performance and support pharmaceutical product quality throughout the container lifecycle.
Improved Packaging Reliability
Testing helps verify that glass containers maintain their integrity and protective function under intended storage and use conditions.
Reduced Product-Container Interaction Risk
Early evaluation of hydrolytic resistance helps identify potential chemical interactions before they affect product quality or stability.
Stronger Packaging Qualification Programs
Generates objective data that supports packaging selection, supplier qualification, change management, and lifecycle packaging control strategies.
