A Mobile Compounding Pharmacy USP 800 Trailer by Odulair, a unit for compounding drugs, is required by the regulatory authorities to meet special rates of air exchanges, different rooms pressurizations, special kinds of wall surfaces, sealing methods and materials, passthrough windows, and more. Mobile pharmacy trailers by Odulair, as well as the mobile compounding pharmacy, the pharmacy mobile clean room, are available for rental, leasing, and sale. Our unique expertise has led us to become the “go-to company” for nationwide and region-wide mobile health outreach programs. We not only provide the mobile clinics per se, but we also provide the mobile health program, technical and logistics expertise to create successful large-scale healthcare operations.

Odulair guarantees USP 800 & USP 797 compliance for your compounding pharmacy. Odulair is owned and operated by a Medical professional. We are the ONLY direct manufacturer of Mobile Pharmacy Trailers, Mobile Compounding Pharmacy. USP 800, Mobile Cleanroom USP 800, Mobile Compounding Pharmacy, Temporary Pharmacy Facilities. Our services include planning, implementing, scheduling regular maintenance, as well as budgeting and finance for your Mobile Pharmacy Trailer. The design we offer meets professional engineer standards at 100% compliance with the USP 800 code for Compounding Pharmacies and Cleanrooms. Odulair takes compliance seriously, ensuring stringent indoor air requirements are followed for your USP 800 Mobile Compounding Pharmacy Cleanroom Trailer.

The United States Pharmacopeia (USP™) is the only independent, non-profit, and non-governmental organization responsible for establishing an inventory of drug and supplement standards. Their main function is to maintain a global catalog of over 4,500 monographs for prescription and over-the-counter (OTC) drugs, dietary supplements, and medical devices.

The USP 800 guidelines developed by the United States Pharmacopeia were created to protect the working environment of pharmacists and technicians when dealing with compounding Hazardous Drugs. This was first published on 9/29/2019, becoming official on 7/1/2018. USP 800 guidelines and standards can vary by State. USP 800 is specific for compounding Hazardous Drugs, while USP 797 is specialized for Non-Hazardous Drugs.

USP 800 also enables the ability to work in a negative pressure environment. All medical equipment comes standard to meet USP 800 cleanroom requirements compliance, excluding floor color. Oftentimes, these units are referred to as a compounding pharmacy or “Clean Room.” This is a room designed to be free from dust and other harmful contaminants using a combination of High-Efficiency Particulate Air (HEPA) filtration air supply in the room. They require a certain amount of pressurization (comparable to an airplane) and a specific number of Air Exchanges per Hour (ACH) to turn air at a constant rate. The cleanrooms are classified into ISO1-ISO9 with the larger the ISO# having more particles in the air. They have been designed as a place for the pharmacist to mix together the exact dosage of ingredients when creating personalized medications.

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