This Division provides analysis and quality assurance to meet FDA Good Manufacturing Practice (GMP) / Good Laboratory Practice (GLP) guidelines.
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Our stability department is ready to design a shelf life testing schedule to determine expiration dating of OTC products. We will consult with you to provide even more rigorous standards to exceed product expectations. We use methods that comply with the Guidance for Industry (Q1A Stability Testing of New Drug Substances and Product.)
This division provides analysis and quality assurance to support EPA product testing requirements. We also provide regulatory consulting to support state and federal product registration.