Pharma Natural

A U.S. Food and Drug Administration
Licensed & Registered Manufacturer

Pharma Natural’s highest priority stakeholders are the persons who consume our products. Established in 2002, Pharma Natural is licensed and registered with the United States Food and Drug Administration Food (FDA). Since its inception the Company has operated in compliance with FDA 21 CFR 111 – CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS and all FDA issued dietary supplement (DS) current good manufacturing practice (GMP) regulations in compliance with the mandate from the Dietary Supplements Health and Education Act (DSHEA). Directed by the FDA’s GMP regulations that require manufacturers to establish their own quality specifications for identity, purity, strength, composition, and absence of contaminants, Pharma Natural Inc. has adopted a continuous process improvement methodology for both its commercial and operational policies, procedures and processes with the objective of being an industry leader in product integrity. The Company operates as required by all FDA mandated regulations and recommended best practices and product quality standards promulgated by the United States Pharmacopeia Convention (USP), consistent with relevant United States Pharmacopeia–National Formulary (USP–NF).

Pharma Natural

Nutriceuticals & Over-the-Counter Body Management Products

The National Safety Foundation is Pharma Natural’s primary, independent professional resource for and has adopted its standards and practices related to all our production and manufacturing processes [NSF’s good manufacturing practices (GMP)]; as well as NSF’s Health Sciences Division’s good laboratory practices (GLP).

NSF International was founded in 1944 from the University of Michigan’s School of Public Health as the National Sanitation Foundation (NSF) to standardize sanitation and food safety requirements. NSF has led the development of more than 70 voluntary American National Standards including dietary supplements to promote public health and safety. NSF/ANSI standards are developed through involvement of stakeholders affected by the standard. The process ensures balanced input from industry representatives, public health/regulatory officials, users/consumer representatives and other relevant interest groups. The NSF Health Sciences Division offers training and education, consulting, auditing, good manufacturing practice (GMP) and good laboratory practice (GLP) testing, certification, R&D and regulatory guidance for the pharmaceutical, medical device and dietary supplement industries throughout the product lifecycle.