Compare CDMOs with GMP microbiology laboratory capabilities for sterility testing, endotoxin analysis, bioburden, and environmental monitoring.
4 companies listed
Microbiology testing ensures pharmaceutical products are free from harmful microorganisms and endotoxins. For sterile products (injectables, ophthalmic), sterility testing and endotoxin analysis are critical release tests. For non-sterile products (oral, topical), bioburden limits and specified organism absence testing protect patient safety.
Environmental monitoring is the ongoing surveillance component of microbiology. CDMOs must continuously monitor manufacturing areas for viable and non-viable particulates, surface contamination, and personnel contamination. Trending environmental monitoring data provides early warning of contamination control issues before they affect product quality.
United Kingdom
Cormica has a proud heritage spanning over six decades, partnering with pharmaceutical, medical device, and combination product manufacturers to accelerate safe, compliant product development and release. From R&D to post-market surveillance , we deliver end-to-end testing solutions across analytical chemistry, microbiology, and physical testing. Our GMP, GLP, and ISO 17025 accredited laboratories across the world ensure global regulatory technical excellence.
Spain
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Portugal
Labfit is a brand of the Portuguese company HPRD Health Products Research and Development Lda, which identifies and communicates the laboratory and regulatory consultancy activities focused on pharmaceutical products, cosmetics, medical devices, biocides and textiles.