Introduzione
Food Supplements in the EU: Advanced Regulatory Assessment
Assessing a food supplement requires connecting information on ingredients, formulation, labelling and marketing communication. When that information is incomplete or a product sits close to the boundary between categories, regulatory review calls for critical judgement and a structured approach.
Building on a working knowledge of EU food supplement regulations, this advanced course focuses on applying requirements to concrete product assessments. Participants will examine potential compliance issues, identify where additional information is needed and discuss possible actions to address the findings.
Practical examples and case studies lead into an interactive workshop in which participants review a complete food supplement package, bringing together formulation, labelling, claims and marketing materials. The emphasis is on explaining assessment findings and identifying appropriate next steps.
Programme
This course will provide:
- Guidance on assessing food supplement ingredients and formulations
- Advanced examples of labelling, health claims and marketing communication
- Insights into complex regulatory and borderline situations
- Practical approaches to identifying compliance issues and deciding how to address the
- Case studies and an interactive workshop based on the review of a food supplement package
Professionals involved in the development, regulatory review or marketing of food supplements, particularly Regulatory Affairs specialists, Quality Assurance and Quality Control professionals, and product developers who need to assess products and address practical compliance questions
Participant experience
This is an advanced course. Participants should have a working knowledge of EU food supplement regulations, including general labelling requirements and the rules on nutrition and health claims.
Interactive teaching combines focused regulatory explanations, practical examples, case studies, quizzes and Q&A.
Docente/i
Enej Å terbenc
Enej began his professional career as a physician. After leaving clinical practice, he joined Billev Pharma East as a Medical advisor. In his current position, he is part of a team ensuring the safety of medical products. He also participates in various projects bringing new products to market.
Online Training – 1 module
06 April 2027 from 2:00 pm to 6:00 pm CEST
After the registration, you will receive all details about the connection.
The course will proceed with a minimum number of participants. Should this number not be reached the registered participants will be notified one week prior to the commencement of the course.
Early Bird: € 535,00* (until 16 March 2027)
Ordinary: € 665,00*
Freelance – Individual – Academy – Public Administration: € 435,00*
* for Italian companies: +22% VAT
The fee includes:Â tuitions, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.
Newsletter
Roberta Alberti
Events & Training Manager
Cosa saprai fare dopo il corso
Online interactive training on Zoom platform.
LS Academy will provide the access link to the virtual platform a few days before the training.
