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Pharmaceutical Export to Vietnam from India

Pharmaceutical Export to Vietnam from India

Pharmaceutical Export to Vietnam from India

Vietnam has a growing pharmaceutical market supported by healthcare demand, local pharmaceutical manufacturing and international pharmaceutical trade. India is an established pharmaceutical trading partner for Vietnam. In 2025, India exported approximately US$166.25 million of pharmaceutical products to Vietnam.

Global Entra Pharma is an Indian pharmaceutical manufacturer offering selected finished pharmaceutical formulations for pharmaceutical companies, distributors and healthcare businesses in Vietnam.

Pharmaceutical Manufacturing for Vietnam

Global Entra Pharma specializes in selected pharmaceutical dosage forms, including:

  • Pharmaceutical suppositories

  • Vaginal pessaries

  • Vaginal ovules

  • Pharmaceutical creams

  • Pharmaceutical ointments

Products can be manufactured according to the required composition, strength, specifications, packaging configuration and applicable Vietnamese regulatory requirements.

Pharmaceutical Regulatory Authority in Vietnam

The Drug Administration of Vietnam (DAV) under the Ministry of Health is the principal authority responsible for pharmaceutical management, including medicine registration and pharmaceutical regulatory procedures.

Vietnam's Ministry of Health provides official administrative procedures covering pharmaceutical product importation and related activities through its national public-service system.

Pharmaceutical Registration in Vietnam

Medicines intended for commercial distribution in Vietnam are subject to the applicable registration and authorization requirements.

Depending on the product, the regulatory documentation may include:

  • Product registration application

  • Manufacturer information

  • Manufacturing licence

  • GMP documentation

  • Qualitative and quantitative composition

  • Manufacturing process

  • Finished-product specifications

  • Analytical methods

  • Certificate of Analysis

  • Stability data

  • Packaging specifications

  • Labelling and package insert

  • CPP, where applicable

  • FSC, where applicable

  • Product samples, where required

The exact documentation depends on the dosage form, product classification and applicable Vietnamese regulations.

Pharmaceutical Import Requirements

Vietnam maintains specific procedures for importing pharmaceutical products. The Ministry of Health's current public-service system includes procedures for pharmaceutical imports and identifies the Drug Administration of Vietnam as the authority for chemical drugs, herbal medicines, vaccines and biological products in relevant procedures.

Import documentation may include:

  • Commercial invoice

  • Packing list

  • Certificate of Origin

  • Bill of Lading or Air Waybill

  • Certificate of Analysis

  • Manufacturing licence

  • GMP certificate

  • Product registration documentation

  • CPP or other regulatory certificates

  • Packaging and labelling information

The Vietnamese importer should verify the current requirements applicable to the specific product before shipment.

Suppositories for Vietnam

Global Entra Pharma manufactures pharmaceutical suppositories for selected therapeutic applications. Different strengths, formulations and packaging configurations can be developed according to the agreed product specification.

Pessaries for Vietnam

Vaginal pessaries provide a specialized dosage form for women's healthcare. Selected formulations can be manufactured with suitable active ingredients, strengths, formulation bases and packaging configurations.

Vaginal Ovules for Vietnam

Vaginal ovules provide flexibility for women's healthcare formulations. Manufacturing can accommodate selected active ingredients, suitable formulation bases, strengths and packaging formats according to the agreed specification.

Pharmaceutical Creams for Vietnam

Pharmaceutical creams are used across dermatological, anti-infective and other topical therapeutic categories. Selected formulations can be manufactured according to the required strength, formulation and packaging specifications.

Pharmaceutical Ointments for Vietnam

Pharmaceutical ointments provide a semisolid dosage form for various topical applications. Manufacturing can be planned around the required formulation, strength, packaging and quality specifications.

Quality and Regulatory Documentation

A suitable technical documentation package supports product registration and pharmaceutical supply. Depending on the product, documentation may include:

  • Manufacturing licence

  • GMP certificate

  • Certificate of Analysis

  • Product specifications

  • Stability documentation

  • Batch manufacturing documentation

  • Packaging specifications

  • CPP

  • FSC

  • Regulatory dossier

Documentation should be prepared according to the requirements applicable to the specific Vietnamese product registration pathway.

Private Label Pharmaceutical Manufacturing

Global Entra Pharma provides private-label manufacturing for selected pharmaceutical formulations. Buyers can specify composition, strength, packaging configuration, artwork and other technical requirements.

Private-label manufacturing enables pharmaceutical companies and distributors to develop products under their own approved brands while utilizing an Indian pharmaceutical manufacturing facility.

Contract Pharmaceutical Manufacturing from India

Global Entra Pharma supports contract manufacturing for selected finished pharmaceutical formulations.

Products can be manufactured according to agreed technical specifications, quality requirements, packaging configurations and applicable regulatory documentation.

For Vietnam, the responsibilities of the manufacturer, product applicant, importer and other regulated parties should be established before commercial supply.

Pharmaceutical Export Process to Vietnam

A typical export process can include:

  1. Product selection

  2. Strength and quantity confirmation

  3. Commercial quotation

  4. Technical and regulatory review

  5. Registration requirement assessment

  6. Dossier preparation

  7. Packaging and artwork approval

  8. Manufacturing

  9. Quality control and batch release

  10. Export documentation

  11. Shipment to Vietnam

The actual process depends on the product, registration status, importer and applicable Vietnamese regulations.

Why Choose an Indian Pharmaceutical Manufacturer?

India is one of the world's major pharmaceutical manufacturing and export centres. Its pharmaceutical trade with Vietnam is well established, with approximately US$166.25 million of pharmaceutical products exported from India to Vietnam in 2025.

For Vietnamese pharmaceutical buyers, manufacturing from India can provide access to specialized dosage forms, private-label production, customized packaging and structured pharmaceutical documentation.

Five Specialized Pharmaceutical Dosage Forms

Global Entra Pharma's specialized manufacturing portfolio includes:

  • Suppositories

  • Pessaries

  • Vaginal ovules

  • Pharmaceutical creams

  • Pharmaceutical ointments

These dosage forms cover applications across women's healthcare, dermatology, anti-infective therapy and other pharmaceutical categories.

Frequently Asked Questions

Can pharmaceutical products be exported from India to Vietnam?

Yes. India exported approximately US$166.25 million of pharmaceutical products to Vietnam in 2025.

Who regulates medicines in Vietnam?

The Drug Administration of Vietnam under the Ministry of Health is the principal pharmaceutical regulatory authority.

Is pharmaceutical registration required in Vietnam?

Pharmaceutical products intended for commercial distribution are subject to the applicable Vietnamese registration and authorization requirements.

Can pharmaceutical products be imported into Vietnam?

Yes. Vietnam has established pharmaceutical import procedures administered through the Ministry of Health and relevant pharmaceutical authorities.

Can Global Entra Pharma manufacture private-label medicines for Vietnam?

Yes. Selected pharmaceutical formulations can be manufactured under private-label arrangements according to agreed specifications and applicable Vietnamese requirements.

What documents may be required for registration?

Depending on the product, documentation may include manufacturing and GMP certificates, composition, specifications, analytical information, stability data, CoA, CPP, FSC, packaging information and product samples.

Pharmaceutical Export from India to Vietnam

Global Entra Pharma manufactures specialized pharmaceutical formulations for pharmaceutical buyers across Asian, African, Middle Eastern and other international markets. Its manufacturing portfolio includes suppositories, pessaries, vaginal ovules, pharmaceutical creams and ointments.

For pharmaceutical export to Vietnam, product registration, importer requirements, import procedures, labelling and technical documentation should be verified according to the current requirements applicable to the specific product.


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