For Us, your health is always first!
Pharmaceutical API Supplier for Vietnam — WHO-GMP Export from India
Aarise Pharma is a WHO-GMP certified pharmaceutical API manufacturer and exporter based in Haridwar, India, supplying bulk active pharmaceutical ingredients and third-party manufactured dispersible tablet formulations to buyers in Vietnam. Every shipment ships with an independent Certificate of Analysis (COA) and full regulatory documentation.
Pharmaceutical API Supplier for Vietnam — Why Buyers Choose India
Vietnam’s DAV oversees one of Southeast Asia’s fastest-growing generics markets. Domestic API manufacturing capacity remains limited, which keeps import dependency on suppliers like India consistently high. Aarise Pharma works directly with pharmaceutical manufacturers, contract formulators, and distributors in Vietnam sourcing bulk APIs from India as an addition to, or replacement for, existing suppliers.
API & Formulation Categories Available for Vietnam
Active Pharmaceutical Ingredients (APIs)
Bulk APIs across therapeutic categories including analgesics, antibiotics, antihistamines, and gastrointestinal formulations, manufactured to USP/BP/EP pharmacopoeial standards.
Dispersible Tablet Formulations
Contract-manufactured dispersible tablets, formulated and packaged to your specification — a core capability of the Haridwar facility.
Third-Party Manufacturing
Full third-party manufacturing for finished dosage forms, from formulation through packaging, for buyers in Vietnam looking to private-label or scale an existing product line.
Quality Documentation We Provide
Every order from Aarise Pharma includes a Certificate of Analysis (COA), Material Safety Data Sheet (MSDS), and WHO-GMP compliance documentation.
Shipping to Vietnam
Standard delivery to Vietnam is 7-12 business days by air freight, 20-28 days by sea. We handle export documentation and coordinate with your customs broker or local registration holder where the import process requires one.
Regulatory Information for Vietnam
DAV (Drug Administration of Vietnam) is the national authority governing pharmaceutical imports into Vietnam. Vietnam’s DAV oversees one of Southeast Asia’s fastest-growing generics markets. Domestic API manufacturing capacity remains limited, which keeps import dependency on suppliers like India consistently high.
Frequently Asked Questions
What pharmaceutical APIs does Aarise Pharma supply to Vietnam?
Aarise Pharma manufactures and exports WHO-GMP certified active pharmaceutical ingredients, dispersible tablet formulations, and third-party manufactured finished products for buyers in Vietnam, including generic drug manufacturers, contract formulators, and pharmaceutical distributors.
What documentation do you provide for DAV compliance?
Every shipment includes a Certificate of Analysis (COA), Material Safety Data Sheet (MSDS), and Drug Master File (DMF) reference details, formatted to support your DAV registration or import filing.
How long does shipping to Vietnam take?
Standard delivery to Vietnam is 7-12 business days by air freight, 20-28 days by sea. We coordinate directly with your customs broker or local registration holder where the import process requires one.
Can Aarise Pharma manufacture a custom formulation for us?
Yes. Beyond bulk APIs, Aarise Pharma offers third-party contract manufacturing for dispersible tablets and other finished dosage forms, built to your specification and packaging requirements.
How do we request a quotation?
Send your required molecule, quantity, and target specification through our contact form, and our export team will respond with pricing, MOQ, and lead time within one business day.
Get Started — Request a Quotation for Vietnam
Send us your required molecule, quantity, and specification, and our export team will respond with pricing, minimum order quantity, and lead time within one business day.
Other Export Markets
Aarise Pharma supplies pharmaceutical APIs to buyers across 18+ countries. See our other supplier guides: