In many cases, the first step in the product development pathway is to understand the safety, efficacy, and claims potential of your ingredient or product. Your business goals, markets of interest, and regional regulatory requirements will dictate the level of depth needed for your scientific evidence dossier.

Our regulatory affairs team has completed hundreds of scientific literature reviews for a wide range of ingredients, product types, dosage forms, dosage routes, and health indications. The resulting dossier will help support your go-to-market strategy or reveal research gaps that require new evidence to be generated, such as through a clinical trial, to substantiate your product’s claims.

Learn how we can help you gather strong supporting scientific evidence that stands up to regulatory scrutiny.