Quality Practices

The following process assures the quality of our products:

• Specifications are set for raw materials and finished products.
• Raw materials are sourced with Certificates of Analysis.
• Products are manufactured using Standard Operating Procedures.
• Products are inspected at our warehouse for damage, label accuracy, appearance, taste and odor prior to release.
• Product is quarantined if failing to pass inspection.
• Products are assayed by independent labs for isotonic capability, micro contamination and potency.
• Manufacturing facilities are audited on a regular basis for GMP compliance. GMP stands for “good manufacturing practice regulations” and these regulations are established by the FDA. GMP requires that manufacturers, processors, and packagers of drugs, medical devices, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective. GMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination and errors.