Sterile and 
Non-Sterile Tests

Pharmetric ensures the sterility, safety, and efficacy of pharmaceutical products with advanced microbial testing. We deliver rapid sterility test results in 5-7 days. Our services include USP <51> Antimicrobial Effectiveness Testing for preservative efficacy, and USP <60>, <61>, and <62> tests to detect microbial contaminants. We also perform growth promotion testing to validate growth media, and 14-day media fill tests to assess aseptic process sterility. Pharmetric’s rigorous standards and advanced methods ensure top-tier microbial safety and quality assurance.

Advanced biological testing services to ensure pharmaceutical product safety and efficacy. Our USP <81> Antibiotics – Microbial Assays assess antibiotic potency using cylinder-plate and turbidimetric methods, measuring zones of inhibition and microbial growth reduction. For endotoxin detection, our USP <85> Bacterial Endotoxin Tests employ chromogenic and turbidimetric techniques. Additionally, we validate dry heat ovens with endotoxin challenge vials to ensure they meet sterilization standards. Pharmetric’s cutting-edge methods guarantee the highest levels of safety and effectiveness for your products.

Our identification methods confirm the identity, purity, and quality of raw materials using advanced techniques such as Infrared (IR) Spectroscopy, Ultraviolet-Visible (UV-Vis) Spectroscopy, High-Performance Liquid Chromatography (HPLC), and Mass Spectrometry (MS). For potency testing, we employ HPLC, MS, UV-Vis Spectroscopy, and titration to verify the appropriate amount of active pharmaceutical ingredients (API) in medications. We also excel in method development and validation, ensuring system suitability, specificity, linearity, accuracy, precision, intermediate precision, robustness, and forced degradation testing to maintain high analytical standards.

At Pharmetric Laboratory, we provide thorough physical testing to ensure the integrity and quality of pharmaceutical products. Our Container Closure Integrity Testing employs methods like Vacuum Decay, Pressure Decay, and Dye Ingress to ensure product safety. We assess appearance and perform USP <791> pH testing to maintain product standards. Our services include testing for subvisible particulate matter in various formulations per USP <787>, <788>, and <789> guidelines. We also conduct USP <697> Container Content for Injections and USP <905> Uniformity of Dosage Units tests, including content uniformity and weight variation, to ensure consistent and reliable dosage.