Indonesia Cosmetic Registration Service
Naviguez dans les réglementations locales complexes grâce à nos conseils d'experts. De l'enregistrement des produits aux services de représentation désignés.
Solutions globales
Regulatory solutions to ensure your cosmetic products are fully compliant and ready for the Indonesia market.
Navigating the complex BPOM (Badan POM) notification system for cosmetic products in Indonesia.
Guidance and assistance in preparing, translating, and reviewing all required notification documents, ensuring full compliance with format and content requirements.
Acting as your liaison with Indonesia’s BPOM and local partners, including importers and manufacturers, to facilitate regulatory communication.
Representation for company registration, account management, and product notification submissions through BPOM’s official electronic system.
Support in handling post-notification matters, including notification renewals, information updates, and product kit notifications.
Interpretation of Indonesian cosmetic regulations, with tailored guidance on product classification, ingredient compliance assessment, and overall notification strategy.
Pourquoi nous choisir ?
Ensure smooth and compliant market entry into Indonesia with strong local expertise.
Regulatory Expertise ⭐
Full-Service Management
Proactive Risk Control
Strong Local Support ⭐
Questions fréquemment posées
Do I need a local representative in Indonesia?
Yes, in most cases, a local Responsible Person or authorized representative based in Indonesia is required to hold the product registration and handle post-market surveillance.
How long does the registration process take?
Standard product review: approximately 14 working days from payment completion (product ID issuance).
Perfume/fragrance products: about 3 working days.
Actual end-to-end time is usually 3–6 months due to document preparation and coordination.
Halal certification requires additional time for document review and on-site inspection.
What are common risks related to documentation?
Notifications may be delayed or rejected if:
GMP certificates are expired or invalid,
Authorization documents are incomplete,
DIP data is insufficient or missing.
What are common ingredient compliance risks?
Products may fail review if they contain:
Prohibited substances under Indonesian regulations,
Restricted substances exceeding allowable limits,
Safety assessments that are incomplete or inadequate.