Global Food Compliance
Intelligence & Solutions

Regulatory Pathways for New Food Ingredients and Additives in Indonesia

premium members free
Arsy Asyafra Nabila
Thursday , 4th Jun 2026
REACH24H
Background

As one of the largest food markets in Southeast Asia, Indonesia offers significant opportunities for market entry and expansion. At the same time, its regulatory framework for food ingredients and additives—overseen by the Indonesian Food and Drug Authority (BPOM)—is complex and continuously evolving. For businesses, a clear understanding of these requirements is essential to ensure compliance, particularly when dealing with new-to-market ingredients and the use of food additives.

This webinar will provide a regulatory-focused overview of these frameworks, along with practical insights to support compliance and facilitate successful product registration in Indonesia.

Notes:
1. The webinar livestreaming is freely available to all users. You are welcome to register for and participate in the webinar.

2. If you can't attend the live webinar, register anyway and we will upload the webinar materials as soon as they're available.

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Contents

1. Introduction to Indonesia's Food Regulatory Framework

  • Overview of Key Regulatory Authorities

  • Regulatory Structure for Food Ingredients and Additives

  • Market Trends & Regulatory Developments

2. Regulatory Compliance for New Food Ingredients and Additives in Indonesia

  • Regulatory Definition and Scope

  • Approval Pathways and Timelines

  • Administrative Document Requirements

  • Technical Data Requirements

3. Key Compliance Strategies and Considerations for Market Entry

  • Regulatory Challenges for Approval

  • Market Entry Considerations & Practical Tips

  • Case Sharing / Practical Examples

4. Q&A 

*The final outline may be subjected to subtle revision

Contact Information

If you have any questions about this webinar, please contact us at:

EMAIL: [email protected]

TEL: +86 (0) 571 8609 4444

Speaker
  • Regulatory Specialist
    Arsy is an experienced Regulatory Affairs with a proven track record in ensuring compliance with local regulations and laws. Strong knowledge of regulatory compliance, product registration, regulatory updates, and project management. She has initial major in Pharmacy, then continued her profession program as a Pharmacist in 2018. She spent over three and a half years of experience in Quality Assurance for Industrial Pharmaceuticals, coupled with an additional two years as a Regulatory Affairs and Import + Project Officer for a Cosmetics Import Office, she has effectively collaborated cross-functional teams and liaising with regulatory authorities. Also, maintaining compliance with regulations throughout the product lifecycle.
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