cGMP FDA

Our Mission

At Xseer Pharmaceuticals, we combine scientific rigor, uncompromising regulatory standards, and operational excellence to deliver high-quality pharmaceutical solutions. As a fully FDA-registered 503B outsourcing facility and cGMP-compliant Contract Development and Manufacturing Organization (CDMO) based in Los Angeles, California, we empower licensed healthcare providers, clinics, hospitals, and biotech innovators with reliable access to premium therapeutics and custom manufacturing services.

We don’t just manufacture products — we build transparent, long-term partnerships that advance patient care and accelerate therapeutic innovation.

Who We Serve

We operate two synergistic business lines designed to meet distinct but complementary needs:

Healthcare Providers & Clinical Practices:

Through our 503B outsourcing facility, we supply high-quality, office-use sterile injectables with predictable availability and direct-to-facility pricing.

Biotech & Pharmaceutical Companies:

Our CDMO services provide end-to-end support—from formulation development and analytical testing to clinical packaging and commercial-scale manufacturing.

A Message From Our CEO

The Purpose Behind Xseer

Manufacturing With Purpose.
Building a Legacy of Care.

I have always believed that the deepest fulfillment in life comes not from what we earn, but from the good we are able to do for others. Financial strength allows an organization to grow and sustain its work, but for me, the true measure of success is the positive difference we make in people’s lives. Helping a patient receive treatment on time, supporting a healthcare professional during a critical moment, and solving challenges that affect patient care provide a sense of purpose that money alone cannot offer.

Our time in this world is limited, and I want to use mine to build something meaningful and enduring—an organization whose ability to help does not end with any one person or leader. My hope is that Xseer will continue addressing patient-care challenges, strengthening access to essential medicines, and improving patients’ quality of life for generations to come.

I believe no patient should have to wonder whether the medicine they need will be available.

At Xseer Pharmaceuticals, a drug shortage is never merely an entry on a list. It can mean delayed treatment, difficult decisions for healthcare professionals, and added uncertainty for patients and families who are already carrying enough.

As an FDA-registered 503B outsourcing facility, one of our most meaningful goals is to help strengthen the nation’s response to essential drug shortages. Working within all applicable regulatory requirements, we aim to build the technical readiness, qualified supply chain, and domestic manufacturing capacity needed to respond responsibly when critical sterile medications are in shortage.

At Xseer, we manufacture medications—but our true purpose is to serve people. Every vial carries someone’s trust, hope, and need for care. We will carry that responsibility with compassion, integrity, and an enduring commitment to improving patients’ lives.

Integrated Capabilities

Xseer delivers a true one-stop solution under strict cGMP standards in state-of-the-art ISO-class cleanrooms:

  • Sterile and non-sterile manufacturing, including injectables, oral dosage forms, and topical preparations
  • Formulation development and optimization
  • Comprehensive analytical testing, including HPLC/UPLC, sterility, endotoxin, and stability testing
  • CMC regulatory expertise and inspection readiness
  • Clinical packaging, labeling, and logistics
  • Shortage-response support where permitted under applicable FDA policy

Our integrated Quality Control laboratory enables faster turnaround for internal production and standalone testing services for external partners.

Featured 503B Portfolio

Our portfolio includes sterile injectable formulations designed to support healthcare providers across a range of clinical applications:

  • Essential Vitamin & Nutritional Therapies
  • Weight Management & Lipotropic Formulations
  • IV Hydration & Wellness Support Therapies
  • Shortage-Response Products Where Permitted

Products are manufactured under cGMP standards using controlled processes, comprehensive batch documentation, traceability systems, and established quality controls.

Why Partner with Xseer Pharmaceuticals

  • Transparency & Trust: Gain direct access to our technical experts and clear visibility into your projects.
  • Cost-Effective Excellence: Our direct-to-facility model eliminates unnecessary intermediaries while supporting responsible pricing.
  • Reliability: Benefit from proactive inventory planning and shortage-mitigation support for clinical partners, alongside scalable manufacturing for pharmaceutical developers.
  • Patient-First Mindset: Every decision is guided by quality, patient safety, regulatory compliance, and continuity of care.

At Xseer Pharmaceuticals, compliance is not a checkbox—it is the foundation of our operations. We are committed to providing consistent quality, clear communication, and dependable support throughout every partnership.

Ready to partner with a manufacturer that understands your requirements? Contact our team to discuss your clinical supply or development program.