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

July 6, 2022

Patent Aspects of Vietnam’s Amended IP Law from a Practitioner’s Perspective

Patent is an essential piece of the amended Law on Intellectual Property (“Amended IP Law”), which was passed by the National Assembly of Vietnam on June 16, 2022, and will take effect on January 1, 2023 (except for the regulation on protection of experimental data for agrochemical products, which will take delayed effect on January 14, 2024).

Among the amended and supplemented contents of the Amended IP Law, there are notable patent-related amendments to Article 60 on assessing the novelty of inventions and Article 96 on grounds for invalidating patent protection titles. We discuss these changes below.

Secret Prior Art Under Article 60.1

A significant amendment to Clause 1, Article 60 of the Amended IP Law on the novelty of inventions is to broaden the scope under which an invention can be considered to have lost its novelty.

For the first time in Vietnam, “secret prior art” –a patent application with an earlier filing date or priority date but published on or after the filing date or priority date of an examined patent application – is introduced as a prior art document.

In the diagram above, at the time of filing of the A2 application, secret prior art A1 has been filed but not yet published, making it inaccessible to the public. At this point, only the A1 applicant and the IP Office are aware of the A1 application.

Under the current provisions of the 2005 IP Law, as amended in 2009 and 2019, the A1 patent application is not eligible to be a prior art document when assessing the novelty of A2. However, based on the “first-to-file principle” and the principle of priority, the IP Office has still had other approaches to bar the patentability of an A2 patent application if there is such an A1 application.

By supplementing the provisions of Article 60.1(b) of the Amended IP Law, the A1 patent application can officially be considered “secret prior art” to assess the novelty of A2. As a result, this amendment provides a more legitimate, direct, and comprehensive tool for assessing novelty using “secret prior art.”

From the provisions of the amended Article 60.1, there are still some ambiguities, such as whether secret prior art is limited to the case where the applicants of A1 and A2 are different (in some countries, secret prior art does not apply if the applicants of A1 and A2 are the same), and whether there is a “domestic limitation,” in which patents filed abroad and not yet published are not considered to be secret prior art in Vietnam. After the Amended IP Law goes into force, the authorities will likely issue more guidance to clarify these ambiguous issues.

Finally, one can see that the provision on the use of “secret prior art” applies only to the assessment of novelty of an invention, not to the degree of inventive step.

New Grounds for Patent Invalidation Under Article 96

Article 96 has been amended to include additional grounds for patent invalidation. The two current grounds are (i) the applicant did not have the right, or did not have the right transferred to him or her, to register the invention, or (ii) the subject matter of the invention did not meet the protection criteria. The Amended IP Law adds the following provisions:

(iii) A patent is invalidated in its entirety if:

  • The patent application is filed in violation of the security control regulations, or
  • The invention is directly created based on genetic resources or traditional knowledge about genetic resources but the patent application does not disclose or incorrectly discloses the origin of the genetic resources or traditional knowledge about genetic resources contained in that application.

(iv) A patent is invalidated in whole or in part if:

  • An amendment expands the scope of the disclosed subject matters or changes the nature of the subject matters claimed in the application;
  • The invention is not sufficiently and clearly disclosed in the specification;
  • The patented invention extends beyond the scope of the disclosure in the original specification; or
  • The invention does not meet the first-to-file principle.

In practice, a number of invalidators have cited these grounds in the past in their patent invalidation requests, but as far as we know, the IP Office has not yet used these factual grounds in any judgment to invalidate a patent. This is the first time that these grounds have been codified in law in Vietnam, which could lead to them being used more often in invalidation requests.

The non-protection of inventions filed in contravention of the provisions on security control is mentioned in the current regulations. However, there are still some unclear and controversial points, such as the identification of “Inventions of Vietnamese organizations and individuals” and “inventions created in Vietnam” as the objects of security control.

The Amended IP Law makes the provisions on security control a basis for invalidating a patent if the patent application is filed in violation of this provision, and it also replaces the above ambiguous terms with a clearer term: “Inventions in technical fields that have an impact on national defense and security, created in Vietnam, and under the registration right of an individual who is a Vietnamese citizen and permanently resides in Vietnam, or of an established organization under Vietnamese law.”

More specific guidelines, however, are still needed to accommodate cases such as inventions partially created in Vietnam; inventions jointly owned by Vietnamese entities and foreign entities; inventions created in Vietnam under the right of registration of Vietnamese entities but transferred to foreign entities before filing, and so on.

The protection of genetic resources and traditional knowledge about genetic resources is provided for in Law on Biodiversity No. 20/2008/QH12, as amended by Law No. 35/2018/QH14. The introduction of regulations on disclosure of genetic resources or traditional knowledge about them in patent applications is in line with the trend of using such resources to create new technical solutions. This provision is intended to add additional measures to avoid the loss of said genetic resources in addition to those provided for in the Law on Biodiversity.

Although not a new concept, the provisions on disclosure of genetic resources or traditional knowledge of genetic resources in patent applications are not mentioned at all in the current IP Law. Therefore, there should be specific guidance on the information to be disclosed in the description, how to assess the disclosed information in the procedure for invalidating a patent based on this ground, etc.

Although mentioned as requirements during the examination of a patent application, the grounds relating to disclosure, amendment of a patent description, or the first-to-file principle have never been recognized as a basis for patent invalidation in the IP Law. It is entirely reasonable to include these grounds for invalidation in the Amended IP Law; however, several parts of the implementation remain unclear, such as the procedure and authority to define a “person of ordinary skills in the respective art.”

Conclusion

In our opinion, the Amended IP Law, which has received a lot of feedback from IP practitioners, is a progressive document that introduces many necessary and reasonable changes for the IP environment in Vietnam. However, there are still some ambiguities that require more clarification and professional advice on how to comprehend and implement these new patent provisions. We believe that the Vietnam IP Office will hold dissemination sessions and discussions on how to apply the Amended IP Law.

RELATED INSIGHTS​ 

July 13, 2026
Indonesia’s Halal Product Assurance Agency (BPJPH) has issued new regulations establishing clearer procedures for imposing administrative sanctions on businesses that violate halal product assurance requirements. BPJPH Regulation No. 2 of 2026 on the Imposition of Administrative Sanctions for Violations of Halal Product Assurance Implementation, issued on June 5, 2026, strengthens Indonesia’s halal compliance framework, as mandated under Law No. 33 of 2014 on Halal Product Assurance and Government Regulation No. 42 of 2024 on the Implementation of Halal Product Assurance. BPJPH Regulation No. 2/2026 also supports the upcoming mandatory halal compliance deadline of October 17, 2026, which will apply to a broad range of products and services, including imported food and beverages, slaughtering products and services, natural and quasi-drugs, health supplements, cosmetics, chemical and genetically engineered products, clothing and accessories, household goods, prayer equipment, stationery, and class A medical devices. Scope BPJPH is authorized to impose administrative sanctions for violations of halal product assurance requirements committed by businesses, halal inspection agencies (LPH), halal auditors, halal product process companion institutions (lembaga pendamping PPH), and halal product process companions (pendamping PPH). The head of BPJPH has authority to determine, cancel, or amend the imposition of administrative sanctions, including upon receipt of objections. This authority covers revocation of Halal Certificates (including foreign halal certificate registration numbers), withdrawal of goods from circulation, freezing of LPH operations, freezing of halal product process companion institutions, revocation of PPH companion institution registration numbers, revocation of halal auditor registration numbers, and revocation of LPH accreditation status. Administrative Sanctions Businesses may be subject to any of the following administrative sanctions: Written warning; Administrative fine; Revocation of the halal certificate, including revocation of foreign halal certificate registration numbers; and Withdrawal of goods from circulation. The regulation sets out the types of violations that may trigger these sanctions, with each
July 1, 2026
Obtaining marketing authorization is a fundamental requirement for bringing pharmaceutical products to the Thai market. Companies must navigate the Thai Food and Drug Administration’s registration procedures while also complying with post-approval pharmacovigilance obligations, licensing requirements for manufacturing and importation, data protection rules, and other regulatory requirements. This guide provides an overview of Thailand’s regulatory framework for pharmaceutical marketing authorization, including available registration pathways, review timelines, application fees, postmarketing surveillance obligations, licensing requirements, exemptions, data exclusivity, freedom of information, and parallel import considerations. It is intended as a practical reference for pharmaceutical companies, regulatory affairs professionals, and others involved in bringing medicinal products to the Thai market. Download the guide below for a concise overview of the current requirements and procedures governing pharmaceutical marketing authorization in Thailand.
June 24, 2026
Patent enablement requirements are provided under Article 102 of Vietnam’s Law on Intellectual Property (IP Law). In particular, a patent specification must “fully and clearly disclose the nature of the invention to such an extent that, based on the specification, a person having ordinary skill in the relevant art can implement the invention.” In pharmaceutical and biotechnology patents, this requirement is more complicated and subject to more rigorous assessment. The Patent Examination Guidelines (Guidelines) of the Intellectual Property Office of Vietnam (IP Office) were amended in March 2026 to introduce Annexes III and IV for the pharmaceutical and biotechnology sectors, in which Annex III provides detailed guidelines on the assessment of specification requirements. These amendments were made under a project for strengthening capacity in industrial property examination between the Japan International Cooperation Agency (JICA) and the IP Office. Annex III provides detailed instructions on how examiners assess enablement in a pharmaceutical or biotechnology application, and offers examples of acceptable and unacceptable descriptions with regard to the enablement aspect. Enablement Requirements in Pharma and Biotech Patents Article 12.7 of Circular 10/2026/TT-BKHCN (Circular 10) adds to the requirements of Article 102 of the IP Law that the description must demonstrate the novelty, inventive step, and industrial applicability of the technical solution. For pharmaceutical composition subject matters, Article 12.9 of Circular 10 sets out that the description must present the results of clinical trials and/or the pharmacological effects of the claimed pharmaceutical composition, and must include at least the following information: Substance/mixture used. Testing method (system) employed. Information on the test results. Correlation between the pharmacological effects obtained from the tests and the application of the pharmaceutical product in the prevention, diagnosis, and treatment of diseases. The Guidelines note that pharmacological study results should be presented in a quantified manner, and pharmacological
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