Dietary supplements are routinely taken by over 68% of Americans. Globally, the nutritional supplement industry has reached over $85 billion in sales—with $25 billion coming from the US market alone. As the industry continues to grow, it is essential for your contract manufacturer to uphold the efficacy, potency, and safety of your finished nutritional supplements in order to ensure the integrity of your product to the consumer. These dietary supplement characteristics are regulated stringently in the US, resulting in high-quality nutritional products that exceed most standards of foreign-regulated markets.

Established in 1989, Robinson Pharma, Inc. is a dietary supplement manufacturer located in Southern California. Our products are sold in various channels and distributed in more than 35 countries. Robinson Pharma, Inc. upholds current Good Manufacturing Practices (cGMP) and US Food and Drug Administration (FDA) compliance by allocating resources that support the quality control of our products. Many of our international customers appreciate the investments we make to maintain our current certifications, which allows them to market their supplements with added value. Third-party cGMP and quality certifications provide assurance to the buyer that the manufacturer follows processes, procedures, and documentation protocols to assure the integrity of every supplement.

The FDA is the main governing body for public health in the United States. They monitor the safety and usage of drugs, cosmetics, and food products including dietary supplements, which are covered under the Dietary Supplement Health and Education Act of 1994 (DHSEA). As one of the top nutritional contract manufacturers in the country, we honor these rules and regulations set up to ensure the public’s health and safety.