Please fill out the form below to view the new USP <797> <800> Cleanroom & Sterile Compounding Catalog.
USP <797> compliance requires that the preparation of pharmaceuticals occur in ISO Class 5 (Class 100) clean room with a buffer area of ISO Class 7 (Class 10,000) plus ante-areas of at least ISO Class 8 (Class 100,000). USP <800> is the new chapter which describes practice and quality standards for handling Hazardous Drugs (HDs) to promote patient safety, worker safety, and environmental protection.
IMS offers products to prevent microbial contamination, eliminate introduction of endotoxins or unintended chemical or physical contaminants. Whether compounding hazardous drugs or working with low-risk compounded pharmaceuticals, our cleanroom supplies can support your controlled environment.
IMS serves the following industries: USP <797> Compliance, USP <800> Compliance, Sterile Compounding Pharmacies, cGMP Compliance – Current Good Manufacturing Practices.
Click here for more information on USP <797> <800> compliance and compounding standards.
If you do not find the product you are looking for or have any questions regarding USP <797><800> products, please contact us at email@example.com.
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