On 3 June 2021, the Indonesian Food and Drug Control Agency released guidance on probiotic products which will be used to:
- Classify probiotic products (as to whether they should be categorised as a supplement, pharmaceutical, or food).
- And to identify the safety and quality of the probiotics as supplements.
Based on this new regulation, new strains of probiotics that have not been approved in Indonesia will still need to submit safety data to grant approval of use before submission for product registration.
Reach out to RegASK to know more about probiotics regulations. Get in touch with RegASK’s experts.
Contact RegASK for more details Read more
Subscribe to the latest regulatory news
Curated newsletters
Relevant industry info
Access expert insights