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Find the latest news and updates about product registration in Indonesia.
Maintaining Halal Compliance for Medical Devices in Indonesia
Introducing Sandbox Kesehatan 2025: A Catalyst for Health-Tech and Medtech Innovation in Indonesia
Halal Audit Process and Approval Timeline for Medical Devices
The Real Cost of Halal Certification in Indonesia And How to Avoid Hidden Fees
Step-by-Step Halal Registration for Medical Devices Indonesia via BPJPH
US Soybean Surplus and Indonesia’s Supply Gap: A Lesson in Food Security and Regulation
Indonesia Tightens Raw Material Safety via BPOM Regulation No. 26/2025
The Hidden Risk Behind “Imported” Supplements in Indonesia’s E-Commerce Market
New BPOM Regulation No. 25 of 2025: What Cosmetic Companies Must Know Before October 2026
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.
Indonesia’s Medical Device Registration Guidelines: Step-by-Step Guide
Medical Device Registration Services in Indonesia: Why Work with Experts is Important
Medical Device Registration in Indonesia: NIE, Risk Classes & Regulatory Strategy
Lock in Low Tariffs: How an HS Code Advance Ruling Can Save Your Bottom Line
Embassy Skipped: The One-Step Apostille Trick Every Indonesia-Bound Company Should Know
Why Halal Certification is Essential for Businesses in Indonesia
Step-by-Step Process to Obtain Halal Certification in Indonesia
Packaging and Labeling Compliance for Food Products
Allowed and Prohibited Substances in Dietary Supplements

Editor's Pick

The one guide we’d hand to any company planning to enter the Indonesian market
Farmakope Indonesia VI Suplemen IV: What Changed and Who It Binds
Food Supplement Registration Articles

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 teams face an immediate wave of ambiguity. Following the official issuance of Farmakope Indonesia VI Suplemen IV, the industry’s response frequently fractures into two costly misconceptions: either over-complying out of caution or assuming complete immunity. The first error stems from […]
Avatar Dr. Fachrurrodji, Sp.PK - October 23, 2026
BPOM Herbal Classification: Is Your Topical Herbal Product a Cosmetic, a Quasi-Drug, or a Natural Medicine?
BPOM Regulation Articles

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
Food Supplement Registration Articles

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

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

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

BPOM Food Registration for Dried, Powdered, and Instant Products: The Category Questions That Decide Your Pathway
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

Fresh from the Regulatory Desk

The latest guides, updates, and rule changes on product registration in Indonesia.
BPOM Food Registration for Dried, Powdered, and Instant Products: The Category Questions That Decide Your Pathway
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
PerBPOM 27/2025 Facility Audit: What BPOM Verifiers Actually Check
Class A, B, C, D: How Indonesian Medical Device Risk Classification Drives Everything Downstream
CPKB Certification PerBPOM 8/2026: Three Traps for Brand Owners Choosing a Cosmetic Maklon
Registering High-Energy Therapeutic Equipment in Indonesia: Proton Therapy, Brachytherapy, and Linear Accelerators
SaMD Registration in Indonesia: How Kemenkes Classifies AI-Based Diagnostics

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
Orthopaedic 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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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

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

One of the most critical missteps foreign manufacturers make when entering Indonesia is treating medical

Registering High-Energy Therapeutic Equipment in Indonesia: Proton Therapy, Brachytherapy, and Linear Accelerators

For most hospital groups and manufacturers, the hardest part of bringing proton therapy, brachytherapy, or

SaMD Registration in Indonesia: How Kemenkes Classifies AI-Based Diagnostics

SaMD stands for Software as a Medical Device: software, including AI-based diagnostic tools and clinical

Orthopaedic Implant Registration in Indonesia: The Class C and D Pathway

A hip prosthesis and a spinal fixation system can sit on the same workbench and

Indonesia IVD Registration: How the Pathway Differs from a Medical Device

Indonesia’s diagnostics market has grown fast enough that many manufacturers now assume an in vitro

CPKB Certification PerBPOM 8/2026: Three Traps for Brand Owners Choosing a Cosmetic Maklon
Technical Person in Charge BPOM: The Staffing Requirement That Can Delay Cosmetic Registration
Cosmetic Ingredient Review in Indonesia: Applying PerBPOM 25/2025 Before Submission
BPOM Registration Hotel Amenities: Why Suppliers Miss Their Contract Deadline

Supplement Registration

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

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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 teams face an immediate wave of ambiguity. Following the official issuance of Farmakope Indonesia VI Suplemen IV, the industry’s response frequently fractures into two costly misconceptions: either over-complying out of caution or assuming complete immunity. The first error stems from […]

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,”

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

Pregnancy Supplement Registration in Indonesia: How BPOM Assesses Your File

Most pregnancy supplement files that stall in Indonesia do not fail on safety. They fail

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