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Find the latest news and updates about product registration in Indonesia.
Probiotic Supplement BPOM Registration in Indonesia: Strain, CFU and Claim Requirements
BPOM Food Registration for Dried, Powdered, and Instant Products: The Category Questions That Decide Your Pathway
PerBPOM 17/2025 Probiotic Assessment: What the New Guidance Asks a Probiotic Dossier to Prove
Farmakope Indonesia VI Suplemen IV: What Changed and Who It Binds
BPOM Herbal Classification: Is Your Topical Herbal Product a Cosmetic, a Quasi-Drug, or a Natural Medicine?
BPOM Supplement Claim Guidelines: What You May Say and What Moves You Into the Drug Regime
Indonesia Halal Deadline 2028: What the New Schedule Means for Your Products
Indonesia Hospital Tender Registration: Why Public Hospital Bids Require an Izin Edar You Do Not Yet Have
PerBPOM 6/2025 Stability Testing for Health Supplements: What Your Dossier Must Show
Need help with Product registration or understanding Indonesia's regulatory landscape?
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Our Blogs

Find the latest news and updates about product registration in Indonesia.

Editor's Pick

The one guide we’d hand to any company planning to enter the Indonesian market
The Complete Guide to Health Supplement Registration in Indonesia for Foreign Exporters
Food Supplement Registration Articles

The Complete Guide to Health Supplement Registration in Indonesia for Foreign Exporters

Why Indonesia Is a Market Worth Getting Right Indonesia is Southeast Asia’s largest economy, home to over 270 million consumers with a rapidly growing appetite for preventive health and wellness products. The health supplement sector is booming, fueled by rising middle-class incomes, post-pandemic health consciousness, and increasing demand for imported nutraceuticals. But here is the […]
Avatar Dr. Hussein H. Mashhour, MD - April 27, 2026
How to Register Cosmetic Products in Indonesia: BPOM, Halal & Import Requirements (2026)
Cosmetic Registration Articles

How to Register Cosmetic Products in Indonesia: BPOM, Halal & Import Requirements (2026)

Class A, B, C, D: How Indonesian Medical Device Risk Classification Drives Everything Downstream
Medical Device Registration Articles

Class A, B, C, D: How Indonesian Medical Device Risk Classification Drives Everything Downstream

Navigating the Indonesian Market: The 3 Key Pathways for Foreign Brands
Industry Insights & News

Navigating the Indonesian Market: The 3 Key Pathways for Foreign Brands

Fresh from the Regulatory Desk

The latest guides, updates, and rule changes on product registration in Indonesia.
Probiotic Supplement BPOM Registration in Indonesia: Strain, CFU and Claim Requirements
BPOM Food Registration for Dried, Powdered, and Instant Products: The Category Questions That Decide Your Pathway
PerBPOM 17/2025 Probiotic Assessment: What the New Guidance Asks a Probiotic Dossier to Prove
Farmakope Indonesia VI Suplemen IV: What Changed and Who It Binds
BPOM Herbal Classification: Is Your Topical Herbal Product a Cosmetic, a Quasi-Drug, or a Natural Medicine?
BPOM Supplement Claim Guidelines: What You May Say and What Moves You Into the Drug Regime
Indonesia Halal Deadline 2028: What the New Schedule Means for Your Products
Indonesia Hospital Tender Registration: Why Public Hospital Bids Require an Izin Edar You Do Not Yet Have
PerBPOM 6/2025 Stability Testing for Health Supplements: What Your Dossier Must Show

Medical Device Registration

Risk classes, MoH registration pathways, and distribution license requirements, explained step by step.

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Indonesia Hospital Tender Registration: Why Public Hospital Bids Require an Izin Edar You Do Not Yet Have

Indonesia hospital tender registration is often where foreign manufacturers make their first major misstep long before any bid is actually written. A public hospital tender can feel like an obvious win, there is a clear buyer, an allocated budget, and precise technical specs. But momentum grinds to a halt the moment the procurement team asks […]

Class A, B, C, D: How Indonesian Medical Device Risk Classification Drives Everything Downstream
Registering High-Energy Therapeutic Equipment in Indonesia: Proton Therapy, Brachytherapy, and Linear Accelerators
SaMD Registration in Indonesia: How Kemenkes Classifies AI-Based Diagnostics
Orthopedic Implant Registration in Indonesia: The Class C and D Pathway

Cosmetic Registration

BPOM notification, ingredient rules, and labeling requirements, minus the guesswork

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How to Register Traditional Cosmetics in Indonesia: Kohl, Henna, and Nail Products

Foreign brands often assume registering traditional cosmetics in Indonesia means the same heavy dossier process

CPKB Certification PerBPOM 8/2026: Three Traps for Brand Owners Choosing a Cosmetic Maklon

Most compliance queries surrounding CPKB Certification PerBPOM 8/2026 don’t originate on the factory floor. Instead,

Technical Person in Charge BPOM: The Staffing Requirement That Can Delay Cosmetic Registration

This guide is for companies planning to act as the notification applicant for cosmetics in

Cosmetic Ingredient Review in Indonesia: Applying PerBPOM 25/2025 Before Submission

This guide is for regulatory affairs staff, formulators, and product managers who need to confirm

BPOM Registration Hotel Amenities: Why Suppliers Miss Their Contract Deadline

This guide is for brand owners, account managers, and procurement teams who supply shampoo, soap,

Cosmetic Notification Holder Indonesia: Who Can Legally Be One, and Why It Matters

This guide is for directors and market-entry managers at foreign cosmetic brands that do not

Supplement Registration

BPOM registration, claim and label rules, and the common pitfalls to avoid before you submit.

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Probiotic Supplement BPOM Registration in Indonesia: Strain, CFU and Claim Requirements

A probiotic supplement is the one health supplement category where the active ingredient can die on the shelf. That single fact reshapes the entire registration file. Because the active is a living organism rather than a fixed chemical dose, BPOM does not assess a probiotic the way it assesses a vitamin. It assesses the organism’s […]

PerBPOM 17/2025 Probiotic Assessment: What the New Guidance Asks a Probiotic Dossier to Prove

A regional brand had its probiotic dossier almost ready when marketing asked for one edit:

Farmakope Indonesia VI Suplemen IV: What Changed and Who It Binds

Whenever a new Ministerial Decree modifying pharmaceutical standards is enacted, regulatory affairs and quality assurance

BPOM Supplement Claim Guidelines: What You May Say and What Moves You Into the Drug Regime

It often starts with a single line in a marketing draft: a promise to “heal,”

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