Sterile Compounding Solutions

 
 

Sterile Compounding

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Compounding pharmacies are a critical, but often overlooked part of the healthcare continuum. Because of their direct impact on patient care, quality and safety are essential throughout these facilities.

Testing and quality standards for US facilities are addressed by the United States Pharmacopeial Convention; USP <797> provides guidelines for facilities in which compounded sterile preparations are prepared, stored and dispensed.

Sterility testing, media fill and monitoring of compounding environments are measures that compounding facilities can utilize to ensure quality and minimize the risk of contamination.

MilliporeSigma has the products and expertise to help guide you through these processes, minimize risk and ensure you comply with USP 797.

Sterility Testing



Sterility TestingSterility testing is required for monitoring all products that are manufactured according to GMP and purporting to be sterile.


Media Fill



Merck:/Freestyle/BM-BioMonitoring/Media-Fills/Biom-Media-Fills-11212013-300x300.jpgManufacturers of pharmaceuticals must document their aseptic production conditions regularly.
 


Environmental
Monitoring


Merck:/Freestyle/BM-BioMonitoring/Environmental-Monitoring/BioM-Environmental-Monitoring-05132014-250x300.jpgOur comprehensive solutions provide the best defense against contamination.