BPOM Registration

BPOM Registration — Regulatory Compliance for the Indonesian MarketBPOM Registration refers to product approval and regulatory compliance requirements administered by BPOM (Badan Pengawas Obat dan Mak

BPOM Registration — Regulatory Compliance for the Indonesian Market

BPOM Registration refers to product approval and regulatory compliance requirements administered by BPOM (Badan Pengawas Obat dan Makanan), the National Agency of Drug and Food Control of Indonesia. BPOM is the official authority responsible for regulating the safety, quality, and labeling of products distributed in the Indonesian market.

Products subject to BPOM control must be registered and approved before they can be legally imported, distributed, or sold in Indonesia.


Regulatory Authority Overview

BPOM operates under the Indonesian government and oversees regulatory compliance for:

  • Food and beverage products

  • Dietary supplements and health foods

  • Cosmetics and personal care products

  • Traditional medicines and herbal products

  • Pharmaceuticals and certain medical-related products

BPOM registration is mandatory and forms a critical part of Indonesia’s market access framework.


Products Requiring BPOM Registration

BPOM approval is typically required for:

  • Packaged food and beverages (including imported products)

  • Functional foods and nutritional supplements

  • Skincare, cosmetics, and personal care products

  • Herbal products and traditional medicines

  • Certain health-related consumer products

Each product category follows a specific regulatory pathway with defined technical, documentation, and labeling requirements.


BPOM Registration Process Overview

A standard BPOM registration project generally includes the following steps:

1) Product Classification and Regulatory Assessment

Initial evaluation to confirm product category, applicable regulations, and registration pathway, including:

  • Product formulation and intended use

  • Ingredient compliance and restrictions

  • Product claims and positioning

  • Import and distribution model


2) Technical Documentation Preparation

Preparation and review of required documentation, which may include:

  • Product formulation and ingredient specifications

  • Safety and quality supporting data

  • Manufacturing information and GMP-related documents

  • Product labels and packaging review (Bahasa Indonesia)


3) Submission and Regulatory Review

Submission of registration materials through the BPOM system, followed by:

  • Administrative review

  • Technical evaluation by BPOM

  • Requests for clarification or supplemental information (if applicable)


4) Approval and Product Listing

Upon successful review, BPOM issues an approval number allowing the product to be legally marketed in Indonesia. The approval is product- and brand-specific and subject to validity and post-market requirements.


Key Compliance Considerations

  • All mandatory labeling must be in Bahasa Indonesia

  • Product claims must comply with BPOM advertising and promotion rules

  • Formula changes, labeling updates, or brand changes may require variation filing

  • Post-market surveillance and compliance obligations apply after approval

Proper regulatory planning helps reduce delays and avoid rejection during review.


Deliverables

Typical BPOM registration deliverables include:

  • BPOM approval number and registration confirmation

  • Regulatory submission records

  • Label and claim compliance review documentation

  • Ongoing regulatory support (if required)

These deliverables support import clearance, distributor onboarding, and market launch activities in Indonesia.


Why BPOM Compliance Matters

Non-compliant products may face:

  • Import rejection or customs delays

  • Market withdrawal or product recall

  • Administrative penalties and enforcement actions

  • Distributor or retailer refusal

BPOM registration is essential to protect brand reputation and ensure sustainable market access in Indonesia.


Start Your BPOM Registration Project

Provide your product details, formulation information, and target sales plan to receive a regulatory assessment and BPOM registration proposal. Our team supports end-to-end BPOM compliance, helping international brands navigate Indonesian regulations efficiently and professionally.


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Certifications We Support

We offer certification solutions for major international markets, including:

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  • UL Certification (North America)

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  • CCC Certification (China)

  • KC / PSE / RCM / SAA and other regional approvals

BPOM Registration — Technical Compliance & Project Implementation

BPOM Registration is a mandatory regulatory approval process administered by BPOM (Badan Pengawas Obat dan Makanan), the National Agency of Drug and Food Control of Indonesia. It is required for products subject to food, cosmetic, pharmaceutical, and health-related regulations before they can be legally imported, distributed, or sold in Indonesia.

Our BPOM service is delivered through a structured, project-based compliance model, focusing on regulatory accuracy, document traceability, and efficient approval timelines.


Regulatory Objective

The objective of BPOM registration is to verify that regulated products meet Indonesian requirements for:

  • Product safety and quality

  • Ingredient compliance and restrictions

  • Manufacturing and sourcing control

  • Labeling, claims, and consumer information

  • Post-market regulatory accountability

Each BPOM project is executed based on product category, formulation, and intended market positioning.


Applicable Product Categories

BPOM registration typically applies to the following categories:

  • Food and beverage products

  • Dietary supplements and health foods

  • Cosmetics and personal care products

  • Traditional medicines and herbal products

  • Pharmaceuticals and selected health-related products

Each category follows a defined regulatory pathway with specific documentation and technical review requirements.


BPOM Project Implementation Workflow

1) Product Classification and Regulatory Pathway Definition

We conduct an initial technical assessment to confirm:

  • Product category and sub-classification

  • Applicable BPOM regulations and guidelines

  • Registration route (imported vs. locally manufactured)

  • Local responsible entity and distribution model

Output: confirmed regulatory pathway and project scope.


2) Ingredient and Formula Compliance Review

A detailed review of product composition is performed to verify:

  • Compliance with BPOM positive and negative ingredient lists

  • Concentration limits and usage restrictions

  • Additives, preservatives, colorants, and active substances

  • Consistency with product positioning and claims

Non-compliant elements are identified early to support reformulation or adjustment.


3) Technical Documentation Preparation

Based on product category, required documentation may include:

  • Product formulation and specifications

  • Safety assessment or supporting data

  • Manufacturing process and GMP-related information

  • Certificates of analysis and supplier declarations

  • Product labels, instructions, and claims (Bahasa Indonesia)

All documents are reviewed for regulatory consistency and completeness prior to submission.


4) Submission and Regulatory Review Management

Registration dossiers are submitted through the BPOM system and managed through:

  • Administrative completeness checks

  • Technical evaluation by BPOM reviewers

  • Response to deficiency letters or clarification requests

  • Ongoing communication to support review progression

Our team tracks review status and coordinates responses to minimize delays.


5) Approval, Listing, and Post-Approval Support

Upon approval, BPOM issues a product registration number that authorizes market distribution. Post-approval support may include:

  • Registration confirmation and record management

  • Change management for formulation, labeling, or branding updates

  • Renewal and variation filing support

  • Post-market compliance and audit readiness guidance


Project Inputs Required

To initiate a BPOM registration project, clients typically provide:

  • Product name, category, and intended use

  • Complete ingredient list and formulation details

  • Manufacturing site information

  • Draft labels and packaging artwork

  • Market and distribution plan for Indonesia

Additional requirements may apply depending on product type and regulatory pathway.


Typical Project Timelines

BPOM registration timelines vary depending on product category, data readiness, and regulatory review workload. A structured implementation plan helps manage expectations and reduce avoidable delays.


Why a Structured BPOM Compliance Program Matters

A technically aligned BPOM project helps ensure:

  • Accurate product classification and scope definition

  • Early identification of regulatory risks

  • Efficient regulatory communication and response

  • Defensible compliance records for audits and inspections

This approach supports sustainable market access and long-term regulatory stability in Indonesia.


Start Your BPOM Registration Project

Submit your product information for a technical regulatory assessment and BPOM project proposal. Our team supports end-to-end BPOM registration implementation, from initial compliance review through approval and post-market support.



Certification Services for Electrical & Electronic Products

Fast, Reliable Compliance for Global Market Access


Get Your Electronic Products Certified for Global Markets

We provide professional certification services for electrical and electronic products, helping manufacturers and brands obtain international approvals quickly and efficiently.

From safety and EMC testing to final certification, we simplify complex regulatory requirements and support your products in entering global markets with confidence.


Certifications We Support

We offer certification solutions for major international markets, including:

  • CE Certification (EU)

  • CB Certification (IECEE CB Scheme)

  • FCC Certification (USA)

  • UL Certification (North America)

  • UKCA Certification (UK)

  • CCC Certification (China)

  • KC / PSE / RCM / SAA and other regional approvals

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