Focus Laboratories Inc. products

USPdetails EM procedures required for compounding pharmacies.  Most state Boards of Pharmacy will audit 503a Compounding Pharmacies to these standards.

Once the bioburden of the medical device is understood, appropriate parameters can be established for assuring device sterility.  Sterility must be verified, and this is typically accomplished by direct immersion of the devices in media and incubation for times prescribed by USP .