Founded in 2012 as a subsidiary of Belcher Pharmaceuticals, BPI Labs has grown into a premier manufacturer of high-quality injectable pharmaceuticals. Headquartered in Largo, FL, we are dedicated to enhancing patient care by ensuring that essential medicines are accessible, reliable, and manufactured to the highest standards.
As a leader in pharmaceutical manufacturing, we specialize in the development, production, and distribution of sterile injectables that support hospitals, clinics, and healthcare providers across the United States. Our commitment to quality, safety, and compliance ensures that every product we manufacture meets the industry’s most rigorous standards.
At BPI Labs, we go beyond manufacturing—we are committed to innovation, scientific excellence, and operational integrity. Through strategic investments in advanced technologies, regulatory compliance, and talent development, we continue to expand our capabilities and meet the evolving needs of the healthcare industry.
BPI’s is one of the most technologically advanced sterile manufacturing facilities in the country. The facility was designed with cGMP adherence in mind. Fully Human-Less Robotic Filling Technology
Our fully isolated, robotic fill-finish suites embody the next era of sterile manufacturing. Guided by cutting-edge science and cGMP rigor, our humanless production lines and one-time-use pathways deliver unmatched safety, speed, and transparency.
BPI is an FDA registered drug manufacturer and 503B outsourcing facility. All our compounded medications follow 21 CFR Part 210 and 211 (cGMP). Our licenses allows us to produce medications that can be sold to clinics, hospitals and pharmacies.
Every batch undergoes rigorous testing in our in-house chemistry and microbiology labs, ensuring the highest quality. We exceed standard cGMP regulations with strict self-imposed guidelines and never rely on third-party C of A. All ingredients are tested upon arrival to meet our stringent QC standards.
BPI Labs, LLC., is committed to provide the highest quality pharmaceutical products in order to satisfy the needs of its clients and the health and safety of its customers, meeting or exceeding the statutory and regulatory requirements.
This is achieved through compliance with current Good Manufacturing Practices, continuous improvement culture, human talent development, strong relationship with clients and vendors, and process optimization.
We operate with a steadfast commitment to quality, compliance, and continuous improvement. Every step we take is guided by three core principles that define our culture and drive our success:
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