This is a two-day seminar in English on the documentary and regulatory requirements for nutritional supplements and medicines.

International experts will cover a range of topics, including requirements for novel foods, health claims, food ingredients, supplements, and medicines. Speakers will also discuss the importance of data protection, the pre-clinical and clinical studies needed to obtain authorization, and associated costs. Attendees will also learn about the opportunities, constraints and planning required to succeed in commercialization, as well as point out experiences from the pharmaceutical industry that can be used on foods.