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Facilities

Pharmalab Enterprises, Inc. is a U.S. Food and Drug Administration (FDA) registered facility, compliant in today's Current Good Manufacturing Practices as described in Title 21 of the Code of Federal Regulations. In 2021, Pharmalab earned NSF International's NSF/ANSI 455-2 Dietary Supplements Good Manufacturing Practice (GMP) certification and NSF/ANSI 455-4 Over The Counter (OTC) Drug Good Manufacturing Practice (GMP) certification. 

Quality and compliant centric practices are the foundation of Pharmalab's success which allow for steady growth and reliable production. 

With an extensive portfolio of over 200 formulations, Pharmalab is able to remain flexible by adopting the latest in Just-In-Time inventory management and employing lean manufacturing practices. All equipment is adjustable and capable of handling various packaging presentations and fill volumes. 

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