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Meet USP 788 Particulate Matter in Injections

USP 788 Requirements and Solution. It’s as easy as 1, 2, 3…

1

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.

Download paper
2

Watch this webinar for an overview of the requirements and a solution

On-Demand Webinar: USP 788 Requirements & Solutions

Learn more and register
3

Get an effective and reliable solution

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

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.

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USP 788 regulatory requirements and solution including particle counter and software

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  • Microbial Samplers
  • BioCapt®Certificates of Analysis
  • Compressed Gases Particle Counters
  • Molecular Monitors
  • Software / Data Management

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Corporate Headquarters
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T. +1-303-443-7100
T. +1-800-238-1801
F. +1-303-449-6870
E. [email protected]

Keep in touch! Receive industry news from us:

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