USP 788 Requirements and Solution. It’s as easy as 1, 2, 3…
Start with this USP 788 overview paper
This paper discusses the requirements laid out by US (USP), European (EP), and Japanese (JP) Pharmacopoeia standards and includes the most recent USP 788 (USP 42 2018), EP 5.1 and JP 17 release information. These standards demand that injectable solutions are effectively monitored for microcontamination, specifically non-soluble particulates.
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SamplerSight Pharma Software
Controls syringe operated samplers and collects data from a LiQuilaz particle sensor. Easy USP 788 calibration. 21 CFR Part 11 Compliant.
APSS-2000 Parenteral Particle Counter
Sizes and counts suspended particulate matter in a wide range of liquids, including parenterals, to meet all current U.S., EU and JP Pharmacopoeia standards.
