Reduce waste and cut down on the number of touchpoints in surgery preparation. Fagron Sterile Service US's ready-to-administer critical care solutions are prepared through cGMP-compliant operations in state-of-the-art DEA and FDA-registered and inspected 503B outsourcing facilities inspected against 21 CFR 210 and 211 for pharmaceutical manufacturing.
All labels clearly display the most important product information. Patient safety is paramount, so Fagron Sterile Services US adheres to all ASTM, DQSA, and ISMP medication and anesthesia labeling standards to improve visualization of the most critical elements: Presentation Specifications, Route of Administration, Storage Requirements, TALLman Lettering, Expiration Dating, and Barcode.
Every facility has different needs. To serve you and the patients who depend on you better, Fagron Sterile Services US proudly offers reliable FDA and DEA inspected capabilities in Sterile-to-Sterile, API-to-Sterile and Biologic compounding. Come see for yourself and schedule a site visit today.
As part of the only vertically integrated pharmaceutical company dedicated to sterile compounding, our 503B facilities drive outsourcing solutions on a comprehensive level across the continuum of care. Learn more about our affiliate companies today.