FTIFTI

Formulation Technology’s 40,000-square-foot facility in Oakdale, California meets the FDA’s GMP requirements for dietary supplement manufacturing, as well as requirements for OTC and prescription drug manufacturing. It also meets requirements mandated by Health Canada and the Medicines and Healthcare products Regulatory Agency (MHRA) of the UK. With the capacity to handle large-volume orders and the flexibility to efficiently manage batches as small as 50,000 tablets, FTI is well suited to support both new product development and ongoing large production runs.

Research & Development

Fully staffed, experienced R & D department to meet customer needs. Our specialists have expertise in all areas of dietary supplementation from ingredient efficacy to chemical profile details to sourcing and substantiation

Materials Procurement Department

Our Materials Procurement Department understands all aspects of ingredient sourcing and purchasing, including cost, potency, purity and chemistry on even the most esoteric of ingredients.

Quality Assurance

Our plant production process ensures products are completed and shipped on schedule, with on-site QA lab equipped and staffed to handle all FDA regulations for dietary supplement, OTC and Rx production.