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Veterinary Product Registration in Indonesia
Expert regulatory services for veterinary product registration in Indonesia.
Veterinary
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 expert services to streamline your veterinary product’s journey to market, guiding you through the approval process from initial submission to post-market surveillance.
Our team works directly with BPOM to ensure your product meets the required safety, efficacy, and quality standards. We handle every step of the registration process, ensuring compliance with local regulations and industry-specific requirements.
Registration Process We Manage
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?
- Dedicated Local Team that focuses on Indonesian regulatory procedures and market dynamics.
- Timely support through the approval process
- Full support from submission to post-market surveillance
- Proven track record in regulatory affairs for veterinary products across 120+ countries
- Understanding of BPOM’s specific requirements for veterinary products
FAQs
How do I start the veterinary product registration process in Indonesia?
Artixio guides you in preparing and submitting all necessary documents to BPOM.
What documents do I need for registration?
You will need product dossiers, clinical trial data, labeling, and manufacturing details.
What is the cost of veterinary product registration in Indonesia?
Costs vary based on the product and submission requirements, and Artixio provides clear cost breakdowns.
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