Artixio

Veterinary Product Registration & Regulatory Services in Indonesia

Expert regulatory services for veterinary product registration in Indonesia. We help with veterinary product approval in Indonesia, offering regulatory consulting, dossier preparation, and submission support.

Indonesia Veterinary Product Approval & Support

Indonesia’s veterinary product market is governed by the National Agency of Drug and Food Control (BPOM), which oversees the regulatory processes for veterinary drugs, vaccines, and medical devices.

Artixio offers Veterinary Drug & Feed Registration Services in Indonesia to streamline your veterinary product’s journey to market, guiding you through the approval process from initial submission to post-market surveillance.

Getting veterinary products registered in Indonesia can be tricky if you’re not familiar with how BPOM works. That’s where we come in. We don’t just fill out forms — we understand what the regulators are really looking for. Our team helps you sort out the paperwork, fix any gaps, and follow through until you get the approval. We stay updated with local rules, so you won’t miss anything that could cause delays. Whether it’s a new product or a change to an existing one, we help you get it done right.

Indonesia Regulatory Process for Veterinary Products

Pre-Registration

Prepare product dossiers, including clinical data and safety profiles

Registration

Submit documentation to BPOM for review and approval

Post-Registration

Ongoing market surveillance, adverse event reporting, and regulatory updates

Why Artixio For Veterinary Product Registration in Indonesia?

FAQs

How do I start the veterinary product registration process in Indonesia?
Artixio guides you in preparing and submitting all necessary documents to BPOM.
You will need product dossiers, clinical trial data, labeling, and manufacturing details.
Costs vary based on the product and submission requirements, and Artixio provides clear cost breakdowns.

Regulatory Expertise Across Multiple Countries

India
Vietnam
Mexico​
Vietnam
United States
Brazil
Europe
Malaysia
Taiwan
China
Thailand
Philippines

Industries we serve

Pharmaceuticals

Cosmetics

Nutrition

Medtech

Biologics

Veterinary

Blogs

COFEPRIS Simplifies Medical Device Registration in Mexico (2025)

COFEPRIS Simplifies Medical Device

New Regulatory Agreement by COFEPRIS for Simplification of Medical Device Registration Procedures and Shorter...

September 24, 2025
COFEPRIS Reliance Pathway: Mexico Regulatory Update 2025

COFEPRIS Reliance Pathway: Mexico

Modernization of the COFEPRIS Regulatory Framework: Introduction of a Reliance Pathway Diario Oficial de...

September 3, 2025
Artificial Intelligence (AI) in Medical Device Regulatory Affairs

Artificial Intelligence (AI) in

The technological possibilities are expanding day by day. One of the biggest proof for...

September 3, 2025