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Regulation requires your pharmaceutical product to undergo USP 788 and USP 789 testing, and we know you’re worried about changing regulations, contamination, and falling behind schedule. We're your Gateway to market!
Discover Gateway
Analytical's Expertise
Consult With Our Analytical Experts About USP <788> and USP <789> Testing Services!
Our USP <788> and USP <789>
Testing Services are Different.
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Our USP <788>
and USP <789>
Testing Services are Different.
Pharmaceutical Particle Analysis Services
Particle size distribution significantly impacts drug product efficacy, which makes ingredient specific particle sizing a requirement for today's regulatory environment.
Medical Device Particle Analysis Services
Particle sizing, counting, and identification analysis provides a detailed accounting of foreign particulate matter present on or within a medical device.
Material Particle Analysis Services
Foreign particulate analysis can identify contaminants hiding in your product materials that impact performance, quality, and safety.
Pharmaceutical Particle Analysis Services
Particle size distribution significantly impacts drug product efficacy, which makes ingredient specific particle sizing a requirement for today's regulatory environment.
Medical Device Particle Analysis Services
Particle sizing, counting, and identification analysis provides a detailed accounting of foreign particulate matter present on or within a medical device.
Material Particle Analysis Services
Foreign particulate analysis can identify contaminants hiding in your product materials that impact performance, quality, and safety.
Gateway Analytical's Automated Particle Testing Services can be performed on organic, inorganic, and metallic materials via:
Method 1 - Light Obscuration
Method 2 - Microscopic Particle Counting
Our industry-leading experts can deliver results that you can be confident in within a matter of hours. We also provide customers with data formats that both comply with USP methods and are also easy to read and understand.
