- Home
- >
- Philippines
- >
- Registration
Product Registration Services in Philippines for Life Sciences
End-to-End Product Registration Services in the Philippines for Life Sciences

Services We Offer
Product Registration Process in Philippines
We help Life Sciences companies register and launch their products in the Philippines. From classification and dossier preparation to regulatory submission and market release, our team supports every step with accuracy and local insight.
Food and Drug Administration (FDA) Philippines
Companies often face delays due to changing requirements, long review timelines, and incomplete submissions. At Artixio, we resolve these challenges by keeping our processes updated, preparing country-specific documentation, and maintaining clear communication with the FDA Philippines throughout the lifecycle.
Registration Lifecycle in Philippines:
- Product classification and local applicability check
- Appoint local authorized representative (if required)
- Prepare country-specific dossiers and technical documents
- Submit application to FDA Philippines via ePortal
- Respond to authority queries or additional data requests
- Obtain Certificate of Product Registration (CPR)
- Importation clearance and product listing (if applicable)
- Post-registration renewals and change notifications
Choose Artixio for Product Registration in Philippines
- Experienced with FDA Philippines requirements
- Local expert partners for on-ground coordination
- Fast-track submissions with accurate documentation
- Support for CPR renewals and amendments
- End-to-end guidance across product lifecycle
- Trusted by global Life Sciences companies
FAQs
Do I need a local representative to register my product in the Philippines?
Yes, most product categories require a Philippine-based entity or licensed distributor for submission to the FDA.
Is a Certificate of Product Registration (CPR) mandatory for market entry?
Yes, a CPR issued by the FDA Philippines is required before commercial sale of regulated products.
What post-registration activities are necessary?
Regular renewals, safety updates, and change notifications must be submitted to maintain product validity in the market.
Still Have Questions ?
Get expert answers tailored to your needs.
Industries We Serve in the Philippines
Expert Regulatory Services To Streamline Compliance

Regulatory Intelligence & Strategy

Medical & Technical Writing

Publishing & Submission

Product Registration

Investigation New Drug Application (IND)

New Drug Application (NDA)

Post Approval Lifecycle Maintenance

Artwork and Label Review

Ad Promo Review
Our Global Reach: Serving Life
Sciences Clients Worldwide

India

Singapore

Mexico

Brazil

Vietnam

Malaysia

Argentina

Colombia

Taiwan

China

Europe

Thailand

Indonesia

Philippines

USA

Japan

Qatar

South Korea
Insights from Artixio - Tips & Articles

In Vitro Diagnostics: Meaning,
The term “in vitro” is a Latin word that means “in glass”. Thus, from...
June 20, 2025

IVD Medical Devices Registration
The in vitro diagnostic in India is regulated by the Central Drugs Standard Control...
June 17, 2025

Pharma Manufacturing Booms in
Once overlooked pharma hub in Mexico's Hidalgo region has gained importance with global market...
June 18, 2025