USP <788>
Method for particle counting in parenteral solutions.
Standard
USP <788>
Active
Method for particle counting in parenteral solutions.
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Equipment for these workflows
Instruments with features that support this standard's requirements. Compliance is achieved by the user organization, not by the equipment alone.
Related articles
3 3 articles
19 Oct 2026
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Parenteral Solutions in Argentina: What Changes Under ANMAT Regulation 5146/2026?
ANMAT Regulation 5146/2026 clarifies the requirements for closed manufacturing systems used in large-volume parenteral solutions. Learn how these requirements relate to pharmaceutical quality control and subvisible particle testing.
13 Oct 2026
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Subvisible Particles in Injectables: Analytical Criteria and Compliance with the Argentine Pharmacopoeia
Technical review of Argentine Pharmacopoeia requirements for subvisible particles in injectables, covering sample preparation, acceptance criteria, analytical limitations and HIAC 9703+ applications.
09 Sep 2026
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Why do some surfactants better protect therapeutic proteins against agitation-induced aggregation?
Protein and surfactant compete for the same air/water interface, and whichever arrives first determines the fate of the batch. Adsorption kinetics, not CMC, correlates with agitation-induced aggregation.
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