Accelerated Sterility Testing with Celsis®
Rapid microbial detection using Celsis® ATP bioluminescence. Sterility results in just 4–5 days versus the traditional 14 — reducing production delays while maintaining USP compliance.
View TestSEP Analytical Labs · Thonotosassa, FL
Sterility you
can verify
in days.
Compendial USP testing for compounding pharmacies and pharma — powered by Celsis® ATP bioluminescence for a 4–5 day turnaround.
Turnaround
4–5 days
Celsis® ATP rapid sterility.
Compliance
USP 61 · 62 · 71 · 85
Compendial and accredited.
Portal
One-click submit
Track every sample online.
Reliable & High-Quality
Microbiological Tests
Microbial Enumeration Tests (USP 61)
Total Aerobic Microbial Count (TAMC) and Total Yeast & Mold Count (TYMC) to quantify contamination in non-sterile pharmaceutical, cosmetic, and personal-care products.
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Tests for Specified Microorganisms (USP 62)
Screens for E. coli, Salmonella, Staphylococcus aureus, Pseudomonas aeruginosa, and Candida albicans to confirm the absence of objectionable pathogens.
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Endotoxin Challenge Vials (ECV)
High-quality ECVs to support depyrogenation validation for pharmaceutical, biotech, and laboratory facilities, verifying sterilization cycle effectiveness.
View TestSterility Testing (USP 71)
ATP Bioluminescence sterility testing for compounded sterile preparations — rapid, reliable, and compendial-compliant options available.
View TestEndotoxin Testing (USP 85)
Detection and quantification of bacterial endotoxins (LPS) from gram-negative bacterial cell walls, ensuring product pyrogen safety.
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Analytical Tests
Stability-Indicating Assay (SIA)
Evaluates potency and degradation of pharmaceutical products under storage conditions to confirm efficacy, safety, and regulatory compliance across shelf life.
HPLC Method Development & Analysis
High-performance liquid chromatography methods tailored to your product — impurity profiling, content uniformity, and stability studies.
FTIR Analysis
Fourier Transform Infrared Spectroscopy for functional-group identification and chemical composition verification. Non-destructive, precise, and compliant.
Potency Testing
Quantifies active pharmaceutical ingredient (API) concentration to confirm product strength and specification compliance.
pH Measurement
Critical for stability and compatibility across pharmaceutical formulations, cosmetics, and personal care products.
Rapid Detection Process
Save time testing with our rapid detection process.
Rapid Testing Results
ATP Bioluminescence detects microbiological contaminants in compounded sterile preparations — fast.
Stay USP Compliant
Meet USP requirements while harnessing cutting-edge technology, without sacrificing safety or reliability.
Access Your Testing
Submit tests in a few clicks and access your data anytime, anywhere through our client portal.
New
Now offering stability studies.
Interested in learning more? Have a question for us? Let's talk about how our expanded stability program fits your product.
Contact Us Today