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Section 503B facilities are FDA-registered outsourcing facilities that can produce sterile injectable compounds without requiring FDA approval of each formulation, provided they adhere to Current Good Manufacturing Practice (CGMP) standards and don't market compounds that are essentially copies of FDA-approved drugs
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These may include: Medical Doctors (MDs) Doctors of Osteopathic Medicine (DOs) Naturopathic Doctors (NDs) (in states where they are licensed to prescribe) Nurse Practitioners (NPs) Physician Assistants (PAs) These professionals are trained to assess your health, determine whether peptide therapy is appropriate, and monitor treatment safely
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