You are using an outdated browser and your browsing experience will not be optimal. Please update to the latest version of Microsoft Edge, Google Chrome or Mozilla Firefox. Install Microsoft Edge

May 14, 2015

Foreign Drug Company and Local Distributor Relationships in Vietnamese Public Drug Procurement

Vietnam Pharma Update

Vietnam’s Drug Distribution Policy

Under its WTO commitments, Vietnam agreed to allow foreign-invested entities (FIEs) to conduct distribution services (i.e., commission agent, wholesale, and retail services) for most types of products, but it specifically excluded “pharmaceutical products and drugs.” Consequently, foreign pharmaceutical producers typically establish legal presence in Vietnam by way of representative offices through which they can conduct marketing activities, and use local drug distributors to conduct sales and delivery of their products.

Drugs in state-owned hospitals are provided through either “internal pharmacy departments” or “hospital pharmacies.” The internal pharmacy departments supply drugs to doctors for treatment of patients and not directly to patients. Furthermore, the departments only provide drugs which have been paid for by the health insurance body through the public drug procurement process. In contrast, hospital pharmacies provide drugs directly to patients and at the patients’ own expense. These pharmacies may provide, along with other types of drugs, the same drugs that are on the list of drugs paid for by the health insurance body, but the patients will pay for them directly.

As of January 1, 2015, participation in health insurance became compulsory for all Vietnamese nationals working in Vietnam. Therefore, winning public drug tenders will play a key role in increasing sales for foreign pharmaceutical companies doing business in Vietnam.

Drug Tenders

There are two ways of conducting public drug procurement in Vietnam: (i) tenders by individual state-owned hospitals and (ii) centralized tenders. Currently, centralized tenders are only conducted at the provincial level, where the provincial Department of Health (DOH) is responsible for organizing the tenders and choosing the winning bids. All hospitals under a provincial DOH are required to use the tender results from the DOH to purchase drugs used in their establishments. Individual state-owned hospitals under the Ministry of Health (MOH) organize tenders and choose winning bids by themselves. However, according to the defined roadmap, centralized drug tenders will be held at the national level starting in 2016 and the MOH, not the DOH, will be responsible for organizing them. There are still no detailed guidelines for centralized tenders at the national level. A possible scenario is that hospitals under the MOH will use the tender results from centralized tenders at the national level, while hospitals under the DOH will continue to use the tender results from tenders at the provincial level.

There are three main tender packages: innovator drugs; generics; and traditional and herbal medicines. The generics package is divided into five sub-packages. Each package/sub-package has only one winning drug. This limits the number of chemical drugs with the same active ingredient which can win tenders to a maximum of six. However, bidders also face the challenges of ensuring adequate supply if they win. Therefore, it is difficult for a bidder with limited capacity to join a drug tender, especially a centralized tender.

Relationship Between Local Distributors and Foreign Drug Companies

Role of local distributors in winning the tender

As FIEs are prohibited from distributing drugs in Vietnam, they cannot be the bidders in drug tenders but must assign local distributors to be the bidders instead. Such appointments are normally governed under distribution agreements. In most cases, this is a mutually beneficial relationship.

The local distributor plays an important role in determining the success of a drug tender. There are three groups of criteria used to select the winning bid, including: (i) price; (ii) technical criteria of the drug (scored on a 100-point scale); and (iii) capacity and experience of the bidder. Although, technically, the capacity and experience of the bidder is evaluated on a pass/fail basis and most bidders can “pass,” in reality, the capacity of the bidder also carries over to the technical criteria group, where 70% of the score is for drug quality and the remaining 30% is ostensibly for “packaging, preservation, and delivery,” but is in fact used to evaluate the capacity of the bidder.

Therefore, foreign drug companies should carefully evaluate the capacity of their distributors to make sure they meet conditions that tenders would require, such as experience in providing drugs to hospitals or the ability to meet required conditions in goods delivery stated in the tender dossier, while also making sure the local distributor has other desired qualities such as the ability to meet the requirements set out in the distribution agreement. In practice, it is often difficult to balance the two factors.

Termination of the distribution agreement prior to fulfillment of tender obligations

After a public tender has been won, the most critical problems arise when there is a termination of the distribution agreement or other breakdown in the relationship between the foreign drug company and its local distributor prior to the fulfillment of each party’s obligations under the tender. When such events occur, the distributor is often unable to supply the products as committed in the tender contract and would be liable to pay compensation under the terms of tender contracts as well as become subject to administrative penalties under the tender laws. The bid solicitors (the bid solicitor in a centralized tender is the DOH, while in a hospital tender it is the hospital) can terminate the tender contract. In theory, they can choose another bidder to replace the previous bidder. However, in practice, bid solicitors generally do not choose this course of action. They simply terminate the tender contract because they have a maximum of five other products with the same active ingredients to use. For the foreign drug company, beyond its loss of profits, if the drugs earmarked for the tender have not been paid for but are in the possession of the distributor, the foreign drug company is likely to have trouble receiving payment and/or getting its drugs back from the distributor.

Therefore, terminating the distribution agreement prior to the completion of performance of a tender contract will cause losses for both the distributors and the foreign drug company. In most cases, the foreign drug companies would have sent at least some of their drugs to their distributor on credit terms, and therefore are likely to suffer more losses than the distributors.

Possibility of switching distributors while the tender contract is active

Under the Law on Bidding, in some circumstances, it is possible for a bidder to transfer a portion of a package to another bidder while the tender contract is still active, provided it is less than 10% of the total tender contract value, and the transferred portion is valued at below VND 50 billion. Thus, in theory, a foreign drug company could switch distributors for a portion of the tender, though it would require the approval of the distributor, as only the distributor (the bidder) is party to the tender contract under the law, and the hospital (the bid solicitor) would also have to approve. However, in practice, with drug tenders, it is nearly impossible to transfer to another bidder, largely because there is no regime governing such transfers in the pharmaceutical area and because hospitals/bid solicitors, as mentioned above, are usually content to rely on their remaining generic product options.

Protective measures for foreign drug companies

Measures that a foreign drug company can take in the context of drug tenders are: (1) carefully selecting its distributors by conducting proper due diligence on their capability to meet tender requirements as well as commercial and compliance requirements (such as FCPA); and, (2) carefully drafting distribution agreements.

At minimum, the distribution agreements should include the right to conduct inspections, allow termination on clearly enumerated grounds, and have a carefully considered damages and arbitration clause. Also, if the distributors also hold the market authorizations for the drugs, there should be a provision in the distribution agreement requiring them to either cancel or transfer the authorizations to another distributor of the foreign drug company’s choosing. However, practical enforcement of this provision is difficult because sign-off from the distributor is required at the time of cancellation or transfer. As a best practice, the foreign company should hold the marketing authorization in their own name, not in the name of the distributor.

RELATED INSIGHTS​ 

June 19, 2026
For the first time, Thailand’s Food and Drug Administration (FDA) has published a consolidated list identifying all substances that have successfully passed its novel food safety evaluation process. The list is a step forward in regulatory transparency, but it also highlights a feature of the Thai regime that food companies often overlook: each approval is tied exclusively to the company that applied for it. A substance’s appearance on the list does not give other companies the green light to use it. This article examines the structure of Thailand’s novel food approval framework, the implications of applicant exclusivity, and the strategic choices it requires of food companies looking to bring novel ingredients to the Thai market. Thai FDA Food Safety Evaluation Framework Notification No. 376 of the Ministry of Public Health requires novel food substances to undergo a food safety assessment, with an exemption only for novel foods manufactured exclusively for export. The framework also encompasses “foods that do not qualify as novel foods” but which present characteristics warranting a safety evaluation, such as differing quality standards, increased serving sizes, or applications in specific food categories, where such changes affect consumption levels, nutritional value, or consumer safety. The recently published list of foods that passed the safety evaluation by the Thai FDA is structured by substance category and identifies the approved company (domestic manufacturer or importer), country of origin, substance name and trade name, approved purpose of use, and date of the Thai FDA’s approval notification certificate. A notable feature of Thailand’s novel food regime is that the approval result is tied exclusively to the company that submitted the application. Publication of the consolidated list does not constitute a general authorization to use the approved substances. The Thai FDA’s approval certificate specifies the approved conditions of use and the requirements
June 17, 2026
Thailand’s new labeling requirements for medical devices, which include for the first time a unique device identification (UDI) requirement for software as a medical device (SaMD), take effect on June 20, 2026. The Notification of the Ministry of Public Health regarding Criteria, Methods, and Conditions on Labeling and Instructions for Use for Medical Devices 2025, which replaces a similar notification from 2020, was published in the Government Gazette on December 22, 2025. To ensure clarity, modernity, and patient safety, the regulation requires domestic manufacturers and importers to provide labels and instructions for use (IFU) that are clearly legible, complete, and free of false or misleading claims. It also permits IFU to be provided in electronic format, such as via QR codes, websites, or other digital channels—directly relevant to SaMD, where physical labels are impractical and electronic presentation is the natural medium. The notification distinguishes two categories for labeling language. Home-use medical devices (for lay users outside healthcare facilities) must have labels and IFU in Thai. Professional-use medical devices may display labels and documentation in either Thai or English. This distinction is significant for SaMD developers: software intended for clinical professionals may use English-language interfaces and IFU, while consumer-facing health applications must provide Thai-language content. Labeling and UDI Requirements Labels and IFU must include, at a minimum: Product name and intended purpose Quantity or volume Name and address of domestic manufacturer or importer Thai FDA approval number Lot, version, or serial number Manufacturing date and expiry date For SaMD, the version number requirement is particularly relevant. The regulation also mandates display of a UDI code for SaMD in risk category 2 (moderate-risk), category 3 (moderate- to high-risk), and category 4 (high-risk), according to Thailand’s medical device risk classification system (which complies with the ASEAN Medical Device Directive and the EU
June 5, 2026
On May 25, 2026, Vietnam’s Ministry of Health issued Circular No. 16/2026/TT-BYT governing free-of-charge medicine support programs for medical establishments (Circular 16). Circular 16 will take effect on July 10, 2026, replacing Circular No. 31/2018/TT-BYT, which currently regulates the same subject matter. Circular 16 introduces several significant changes compared to the existing legal framework. Removal of Prior Approval Requirement Under the current regulations, free-of-charge medicine support programs are divided into two categories: (1) entirely free-of-charge provision of medicines for all types of drugs and (2) partially free-of-charge provision applicable only to brand-name drugs under patent protection or drugs whose generic products with identical active ingredients and dosage forms are available in Vietnam. Under the current regulations, partially free-of-charge programs are subject to mandatory registration with the competent authority, while entirely free-of-charge programs could be implemented without prior approval. A key reform under Circular 16 is that it stipulates only entirely free-of-charge medicine support programs applicable to all types of medicines, thereby eliminating the partially free-of-charge category. In addition, free-of-charge medicine support programs may be carried out solely based on a written agreement between the pharmaceutical company and the medical establishment, without any requirement for prior approval from competent authorities prior to implementation. Written Agreement Requirements Circular 16 requires the pharmaceutical company and medical establishment to enter into a written agreement in accordance with a prescribed template. This agreement must include the following compulsory information: Information on the supported medicines Form of support (entirely free-of-charge provision to patients) Quantity of medicines provided Target patient groups and applicable indications Duration of the program Rights and obligations of each party Transitional provisions on the protection of patients’ rights upon completion of the program The agreement may contain other contents as agreed by the parties, provided that these do not contradict applicable laws.
June 4, 2026
Indonesia’s Minister of Health has issued Decree No. HK.01.07/MENKES/301/2026 on the Affixation of Nutritional Labels and Health Information to Ready-to-Eat Processed Food Products. The decree came into force on April 14, 2026, and was issued to implement the Health Law and Minister of Health Regulation No. 3 of 2026 on Disease Control. The decree requires the inclusion of Nutri-Level labeling on the front-of-pack nutrition labeling (FOPNL) to indicate the product’s nutritional level based on the content of sugar, salt, and fat (“gula, garam dan lemak (GGL)”). Changes from 2024 Draft Regulation The Nutri-Level labeling was previously proposed in 2024 by the Indonesian FDA (BPOM) through a draft regulation concerning nutrition information. While the categories of Nutri-Level labeling remain the same in the issued decree, the content requirements of sugar, salt and fat in the decree are different from the earlier proposal introduced in the 2024 draft BPOM regulation. In addition, the decree has further specified that the content of fat in the Nutri-Level labeling is the content of saturated fat, not total fat as previously proposed in the 2024 draft. The decree requires Nutri-Level labeling to be implemented in beverage products, which is the same as previously proposed in the 2024 draft BPOM regulation. Other food products may gradually become subject to mandatory Nutri-Level labeling under future implementing regulations. Nutri-Level Labeling Food levels as shown by the Nutri-Level labeling are classified into four color-coded categories from A to D: Level A (lowest amount) in dark green Level B in light green Level C in yellow Level D (highest amount) in red The Nutri-Level labeling is represented by the following image. The requirements for each level for sugar, salt, and fat content, based on amounts per 100 milliliters of product in beverage form, are as follows. Nutri-Level information must be