About Us
Our Story
Medi-Fare Drug prides itself on being one of the first compounding pharmacies to voluntarily register with the FDA as a 503B Outsourcing Facility.
What began over 30 years ago as a retail pharmacy serving local patients and hospitals has evolved into a business that, for the last decade, has focused solely on providing sterile medications to hospitals, physicians, and clinics.
Medi-Fare Drug is committed to providing our partners with products of the highest quality and excellence in customer service.
We are driven by values
Medi-Fare Drug has a custom designed and constructed state of the art clean room that is specifically suited for the cGMP production of a wide variety of sterile products including admixtures, ophthalmics, and diagnostic agents. We also prepare a variety of specialized drug shortage medications, all of which can be multi-dose, unit-dose, or preservative-free.
Our meticulous attention to detail, from environmental testing and cleanroom sanitization, to real-time particulate monitoring ensures sterility is maintained and that quality is by design. Medi-Fare is excited to have recently expanded its facility by constructing a 335 square foot vault in order to increase product volume, which was certified by the DEA in January 2023.
All of our preparations undergo rigorous testing by third-party, independent laboratories, evaluating a wide range of criteria like potency, sterility, pyrogens, stability, and fungi.
Quality
Medi-Fare Drug is committed to providing our customers with quality products and exceptional customer service.
- cGMP validated processes, equipment, and facility
- Using only tested materials from FDA-registered facilities
- Trained, experienced, and tested staff
- Checking and rechecking of preparations
- Quality control unit oversight, documentation, and testing
- Quality control unit oversight, documentation, and testing
Safety
Medi-Fare Drug has all the processes in place to ensure product safety, including:
- Fourteen years of pharmacy-based compounding experience
- State of the art cleanroom
- Ongoing staff training and education
- Environmental and personnel testing
- Process validation
- Third-party, rigorous API and end-product testing
- Certificate of analysis verification