About PharMEDium

PharMEDium is the leading provider of pharmacy-outsourced, ready-to-use compounded sterile preparations (CSPs). With over 20 years of experience, PharMEDium operates 4 state-of-the-art, large-scale, 503B Outsourcing Facilities which are registered with the U.S. Food and Drug Administration (FDA) and state Boards of Pharmacy nationwide.

PharMEDium’s commitment to advancing patient safety is embodied through first-in-class labeling, packaging, and cutting-edge scanning technologies designed to help reduce the potential for medication errors. We help meet the demands for hospitals and Ambulatory Surgery Centers (ASCs), making sure their patients receive their medications on time and as prescribed.

Our more than 1,000 employees (including over 350 pharmacists, certified pharmacy technicians, microbiologists, and chemists) at our Chicagoland headquarters and four outsourcing facilities in Mississippi, New Jersey, Tennessee and Texas are devoted to providing the highest quality compounded drugs. With our focus on continuous, ongoing training, you are assured that PharMEDium products meet or exceed not only Federal and State regulations – but yours as well.

Every square foot is dedicated to quality.

PharMEDium has four large-scale compounding centers, in addition to our Chicagoland headquarters. With more than 280,000 of total square feet of space in our compounding centers and over 10,000 square feet of ISO Class 7 clean room compounding space in these facilities, we have the space and capability to produce the compounded drugs you need – and backup redundancy in the event that one of our facilities is unavailable.

State-of-the-art facilities that meet and in some cases exceed regulations

Each of our compounding facilities is designed to provide high-quality preparations following FDA 503B requirements and state requirements. We meet, and in some cases surpass, the minimum guidelines for clean room design, operation and maintenance to ensure we prepare the highest quality preparations possible.

From the use of minimum ISO 7/Class 10,000 clean rooms to our detailed environmental monitoring and sanitization, we utilize a process for compounding sterile preparations that meets, and in some cases exceeds, all appropriate guidelines and regulations.

We do it through:

  • Monitoring Environment controls include the practice of continuous dynamic monitoring of the facility and clean room environment for temperature and air quality.
  • Sanitization Adherence to a strict regiment for the sanitization of the ISO 5/Class 100 and ISO 7/Class 10,000 Laminar Air Flow Workbench (LAFW) clean room compounding fixtures, floors, walls, ceiling and equipment ensures sterility is maintained at every step of the process.
  • Design Facility design creates a unique environment able to ensure the correct flow for compounding sterile admixtures that significantly reduces the potential for contamination or process error.

PharMEDium commits to quality by design, compliance with FDA guidelines, upholding the highest ethical standards, and supports the best clinical care and patient safety in the industry.  PharMEDium is registered with the FDA and DEA, holds Board of Pharmacy in-state and out-of-state licenses, adheres to applicable cGMP requirements and meets and in many instances exceeds USP Chapter <797> requirements.

Vision and Mission

At PharMEDium, we are committed to patient safety. We take extraordinary measures to ensure the safety and sterility of our services.

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Team

PharMEDium’s commitment to patient safety and quality excellence starts at the very top of our organization and flows throughout all of our associate employees and facilities.

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Careers

PharMEDium is growing. When you work with us, you’re looking at a career, not just a job.

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