Artixio

Veterinary Products Compliance Consulting Services In Malaysia

Veterinary Product Approval & Regulatory Support in Malaysia

Support for veterinary product registration, approval & compliance, import permits, and post-approval changes in Malaysia. We help companies manage regulatory interactions with DVS, NPRA, and other local bodies.

Regulatory Services for Veterinary Products in Malaysia

Malaysia’s veterinary product regulation is primarily managed by the Department of Veterinary Services (DVS) under the Ministry of Agriculture and Food Security. For certain veterinary biologics and combination products, the National Pharmaceutical Regulatory Agency (NPRA) may also be involved.
At Artixio, we provide end-to-end regulatory support for all types of veterinary products, including

Product Types We Support

Malaysia Veterinary Product Approval & Compliance Support

Step What Artixio Supports
1. Product Classification Determine if the product is under DVS or NPRA scope
2. Gap Assessment Review ingredients, formulation, labeling
3. Dossier Preparation Prepare and compile VICH- or ASEAN-format dossiers
4. Submission & Liaison Handle submission to DVS / NPRA and follow-up
5. Import License Assist in obtaining import permits and product listing
6. Post-Approval Changes Support renewals, formulation updates, and claims changes

Why Artixio for Veterinary Regulatory Services in Malaysia?

FAQs

How do I begin the registration process for veterinary products in Malaysia?
Artixio helps identify regulatory pathways and required documentation specific to your product type.
The documents include product dossiers, labeling, safety data, and manufacturing details.
The approval timeline can vary based on the product type and completeness of the submission.

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

Orphan Drug Designation in South Korea (MFDS)

Orphan Drug Designation in

Orphan Drug Designation (ODD) is regulated by Ministry of Food and Drug Safety (MFDS)...

November 4, 2025
Prioritizing Genes from Publicly Available GWAS Summary Stats Using AI

Prioritizing Genes from Publicly

Artixio has developed an artificial intelligence based solution generating a list of prioritized genes...

October 13, 2025
CDSCO Simplifies Subsequent Importer Process for Medical Devices & IVDs

CDSCO Simplifies Subsequent Importer

India’s regulatory authority, the Central Drugs Standard Control Organization (CDSCO), has published an important...

October 3, 2025