Introduzione
This course gives a clear and practical overview of the EU rules for food supplements. Participants will learn about regulatory requirements, including compliance, labeling, and rules on health claims.
It is designed for professionals in regulatory affairs, quality assurance and product development who need to ensure that food supplements follow both EU and national regulations. The course also compares EU, US, and Canadian rules, helping participants understand key differences and best practices.
Through an interactive lecture, examples, and discussions, participants will gain confidence and practical skills to avoid mistakes and ensure compliance with food supplement regulations.
This course will provide:
- An introduction to food supplements
- An overview of the EU food supplement regulatory landscape
- Comparison between EU and US/Canada regulations
- Guidance on the appropriate labelling and health claims
- Insights into the similarities and differences with other product categories
- Practical examples to build understanding and confidence in the knowledge
Regulatory Affairs Specialists, Quality Assurance and Quality Control Professionals, Product Developers and others interested in the basics of food supplement regulations and requirements.
Participant experience
This is an introductory course, and no previous experience is required.
Interactive lecture that includes Q&A, quizzes and practical examples to build understanding and confidence in the newly gained knowledge.
Docente/i
Lara Šterbenc
Lara holds a Master’s degree in Pharmacy and began her career as a Regulatory Affairs Manager at Krka d.d. Novo mesto, overseeing compliance and regulatory processes for various EU and non-EU markets. She transitioned to Billev Pharma East, where she continues her work as a Regulatory affairs manager. Her work covers all aspects of regulatory affairs with a current focus on EU markets.
Enej Šterbenc
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
23 June 2025 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: € 515,00* (until 6 June 2025)
Ordinary: € 645,00*
Freelance – Individual – Academy – Public Administration: € 435,00*
* for Italian companies: +22% VAT
The fee includes: tuitions, organizational office assistance, teaching materials and attendance certificate that will be sent after the training via e-mail.
Newsletter
Registrati
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.