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Southeast Asia snapshot – Changes in patent practice in 2024

Published
11 April 2025
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Authors
Karen Bentley

Karen Bentley

Principal, Melbourne, Singapore | BAppSc (Hons), PhD, MIP Law
Desmond Tan

Desmond Tan

Principal, Singapore | BEng (Hons)
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Patent practice around the world constantly evolves due to legislative changes, policy changes and/or developments in case law. Keeping a keen interest on significant developments in patent practice in Southeast Asia is critical to providing better strategic guidance in relation to our practice. We provide you with a snapshot of the key changes that occurred in 2024.
Country Key Changes


Singapore

Procedure and/or Practice

  • In August 2024, IPOS announced a pilot program through which applicants can seek an extension of 18 months to request search and/or examination without incurring any official extension fees. These fees used to be USD170/month so this is a substantial saving, presumably intended to motivate applicants to delay their examination requests. To benefit from this pilot program, the statutory due date to file the request for examination (which may be filed together with a PPH request), or the request for combined search and examination, must fall between 1 September 2024 and 31 August 2026 (both dates inclusive).
  • Singapore’s Health Products (Therapeutic Products) (Amendment) Regulations 2024 came into effect on August 1, 2024. Effectively a patent linkage system, the legislation requires patent information be provided to the Health Sciences Authority (HSA) during the registration of therapeutic products. The legislation clarifies that only the following patents will need to be declared:
    1. a patent containing a claim for an active ingredient of the relevant therapeutic product;
    2. a patent containing a claim for a formulation or composition of the therapeutic product; and
    3. a patent containing a claim for the use of an active ingredient in the manufacture of the therapeutic product for a specific therapeutic, preventive, palliative or diagnostic use
  • IPOS issued the Supplemental Guidance for the Examination of AI-Related Patent Applications in October 2024, providing additional clarity on how AI-related inventions are assessed. The Guidance includes a set of hypothetical AI applications accompanied by exemplary patent claims and provides a practical reference for applicants as to what examiners are looking for and the examination approach they will take.
  • IPOS has proposed working towards issuance of a first written opinion within 10 months of a PPH request (unknown implementation date). The implementation of mandating such a timeline on IPOS suggests that IPOS would rely more on the assessment (by the counterpart patent office) of the granted patent of the PPH request in order to meet this 10 month deadline.
  • Mandating for patent specification/abstract submissions to be submitted in DOCX format (unknown implementation date), similar to the initiatives at the United States Patent and TM Office (USPTO) and the European Patent Office (EPO). Consequently, IPOS are expecting patent specification/abstract submissions to be directly read and processed by a computer for both time and labour efficiencies at IPOS.
  • IPOS has established a Collaborative Search and Examination (CS&E) Programme with the Indonesian patent office (DGIP) that commenced on 2 January 2025. The programme, which complements the existing CS&E program with Vietnam, provides applicants with a joint CS&E report that represents the opinions of both IPOS and DGIP within 10 months of the examination request at IPOS. The first CS&E report is the official report; but applicants can use the joint CS&E report to expedite examination at the second patent office.


Indonesia

Procedure and/or Practice

  • The Indonesian Patent Office enacted substantial changes to their patent legislation in October 2024. The main changes are:
    • Patentable subject matter. The existing inconsistencies as to the allowability of “second medical use” inventions and computer implemented inventions has been confirmed in the affirmative, thanks to a broadening of the definition of “invention” including the removal of the exemption for patenting “new uses” and “new forms”.
    • Bolar provisions. There are now more generous research exemption provisions allowing testing, use and manufacture of a patented invention for research and experimental purposes to secure regulatory approval. The Bolar Provision is no longer restricted to the five-year period before the patent’s expiration.
    • Patent prosecution efficiencies. Broadly, grace period to exclude public disclosures have been extended from 6 to 12 months, restoration of priority claims is now available within 16 months of the earliest priority date, expediting applications is now also available including expediting publication requests, and there is now the ability to reinstate an application within 6 months of it lapsing.
    • Re-examination of applications is also possible and may be requested by the applicant/patentee or third parties. Importantly, this mechanism can be utilised to (i) continue prosecution after a Notice of Rejection is issued; and (ii) correct allowed/granted patents. To do so however, the request for re-examination must be filed within nine months from the date of issuing the Notice of Rejection or Allowance respectively .
    • Post grant annuity efficiencies. There is now an as-of-right grace period of 6 months to pay annuities with a penalty payment amounting to the outstanding annuity amount.
    • Patent use. There is now a need to provide an annual statement of use, although there is currently uncertainty in relation to consequences for not submitting such a statement.


Malaysia

Case Law

  1. Kendek Products SDN BHD vs DIP Chain Manufacturing SDN BHD, 11 January 2024

    This was an infringement/invalidity case. An interesting element of this case was a challenge by the Defendant as to the Plaintiff's locus standi to bring patent infringement proceedings.

    The issue regarding standing of the Plaintiff (Kendek) to bring the infringement proceedings centred on the validity of an assignment from Kendek Industry Sdn Bhd (“Kendek Industry”), to Kendek Products Sdn Bhd.

    The entirety of the Defendants case was that the regulations require “Form 6” to be filed. Form 6 was filed but it was only signed by the assignee – not the assignor. But the court concluded that “the absence of a counter-signature by Kendek Industry alone does not invalidate the Form 6 or assignment of Patent 342 from Kendek Industry to the Plaintiff”. Moreover, the Court took a very pragmatic approach to the analysis including the intention of the Plaintiff (as the assignee) to accept the assignment.

  2. Sage Therapeutics, Inc v Registrar of Patents, 7 May 2024

    This case relates to a request by an applicant seeking an extension of time to reply to an Examiner’s Report under Section 30 of the Patents Act (“Act”). The Plaintiff missed the response deadline for an adverse examination report, and had applied for reinstatement and an extension of time of 8 months under Regulation 53, citing human error. However, the Registrar denied the request pursuant to new regulations limiting extensions of time under Regulation 53 to 6 months.

    The Court ruled in favor of the Plaintiff and that, its patent application be reinstated and it be granted a one-month extension of time to provide its response.

    But in arriving at that conclusion, The Court rejected both parties submissions. Instead, the Court proceeded on the basis of a different provision that permits a one-time extension without a specific time limit for responding to an adverse report. The Court also found that the Registrar could apply the relevant provisions relating to submitting responses more generously.

Procedure and/or Practice

  • MYIPO has added the Intellectual Property Office of Singapore (IPOS) as a PPH option.


Philippines

Case Law

  1. Kyowa Hakko Bio Co., Ltd. v. Director of Bureau of Patents, Appeal No. 01-2022-0002, 21 February 2024

    Kyowa Hakko Bio Co., Ltd. ("Applicant") filed Patent Application No. 1-2015-501602 entitled "Agent for Elevating Nitric Oxide Concentration".

    An office action was issued by the examiner, and the applicant had requested two, separate two-month extensions, to submit a response, but the examiner only granted the first request, and a second single month extension.

    The applicant filed its response late by one month, and a Notice of Withdrawn Application was subsequently issued by the examiner. The applicant filed a petition to revive its patent application which was denied.

    The applicant appealed the Order denying its petition of revival, seeking to rely on “accident or excusable negligence”. It also submitted that administrative bodies exercising quasi-judicial functions may relax requisite rules in the interest of justice.

    The appeal was dismissed as it was maintained that it was erroneous of the applicant to rely on an automated docketing system since there is no guarantee that a full two month extension is always granted. It was also maintained that that the liberal interpretation of rules does not apply in patent cases due to adverse effects on third parties.

  2. Société Des Produits v. Director of Bureau of Patents, Appeal No. 01-2023-0003, 15 March 2024

    Société Des Produits Nestlé S.A., ("Applicant") filed a request for the National Phase Entry Application of its invention entitled "Nutritional Compositions and Infant Formula for Promoting De Novo Myealination".

    An office action was issued and the applicant had requested two, separate two-month extensions, to submit a response, both of which were granted.

    However, the applicant was filed its response one day past the extended deadline. As a result, a Notice of Withdrawn Application was issued due to the applicant’s failure to submit the response within the extended period.

    The applicant filed a Petition for Revival of Withdrawn Application alleging that the response was inadvertently submitted late by one day and that it had no intention to abandon the patent application. The Petition was denied due to the lack of any reason for the failure to file a response in a timely manner.

    On appeal, the applicant raised the interest of substantial justice to request that the Rules be relaxed and the revival of its patent application be reconsidered. The applicant also submitted that since it was only able to give final instructions at the end of the day of the deadline, the applicant's agent inadvertently only acted on the instructions on the following morning. The applicant argued that such negligence on the part of the patent agent indicates excusable negligence that may be considered for the revival of the application.

    It was held that the agent’s failure to file a response on the due date did not constitute "excusable negligence". Such failure in monitoring deadlines is inexcusable negligence particularly since the original due date for filing a response was already extended twice at the request of the applicant. It was also pointed out that in view of IPOPHL’s 24-hour online filing system, the agent could have still filed the response on the same day it received instructions from the applicant.

    However, the appeal was allowed the patent application revived on the basis that the deadline was missed during the pandemic. Under the circumstances, it was ruled that applicant could be excused from strictly complying with the requirements of the office action.

  3. F. Société Des Produits v. Director of Bureau of Patents, Appeal No. 01-2023-0004, 15 March 2024

    Société Des Produits Nestlé S.A., ("Applicant") has a parent patent application ("Parent Application") which had a Substantive Examination Report where a unity requirement was raised and the subject matter was categorised into Groups I-VI.

    The applicant elected Group I for prosecution and could include the non-elected claims in a divisional application by the deadline.

    The applicant filed a divisional application beyond the deadline and the divisional application was subsequently declared invalid.

    Thereafter, the applicant appealed on the basis that the time extension granted for filing a response for the parent application should also extends to the due date for filing a divisional application.

    The appeal was denied and it was ruled that a separate request to extend the deadline to file divisional application should be submitted. It was ruled that a request(s) for an extension of time to submit a response for the parent application was not a request to extend the filing date of the divisional application.

Procedure and/or Practice

  • The Philippines adopted the WIPO Treaty on Intellectual Property, Genetic Resources and Associated Traditional Knowledge (“Treaty“), which requires the disclosure of information in patent applications whose inventions are based on genetic resources and traditional medicine.
  • Specifications of PCT applications that are filed into Philippines may be filed manually if their length exceeds 250 pages.
  • A framework to provide a list of recognised patent representatives who may conduct business with IPOPHL has been implemented, and twenty four months have been provided for interested parties to comply with the framework for inclusion in the list.


Thailand

Procedure and/or Practice

  • In December 2024, the Department of Intellectual Property (DIP) of Thailand introduced significant updates to the country’s patent framework. The draft was open for public comments until January 31, 2025.

    Key proposed changes include:

    1. increased official fees
    2. late submission of translations will be allowed upon payment of a surcharge fee of approximately USD 90
    3. a shortened First Publication period – proposed to be 18 months
    4. a reduced timeframe for requesting substantive examination from 5 years after publication to 3 years from the filing date
    5. formalized third-party observations
    6. a second publication stage post-examination with the opposition process now taking place at this stage, replacing the current opposition period following the first, pre-examination publication
    7. removal of mandatory foreign examination result submissions, and
    8. the introduction of special export licenses for medicines.
  • The DIP’s Target Patent Fast-Track program, originally launched in 2022, was further expanded in December 2024 to include Green Innovations. The program covers six categories of innovations, as outlined below:

    1. Water and Air Management Innovations
    2. Clean Energy Innovations
    3. Transportation Systems and Electric Vehicles
    4. Green Architecture Innovations
    5. Plastic Alternatives
    6. Waste and Sewage Management Innovations


Vietnam

Procedure and/or Practice

  • On 24 June 2024, the National Assembly of Vietnam approved the amended Law which included the establishment of a Specialized IP Court. Judges working at the Specialized IP Court are required to have professional knowledge and experience in the field under its jurisdiction.


Myanmar

Procedure and/or Practice

  • Patent law came into force on 31 May 2024. The law provides for protection under patent rights and utility model rights.
  • Myanmar is not a PCT country so patent applications must be filed within one year from the date of the first application.
  • Patent applications can be filed in English or Myanmar language, but the registrar may request the submission of a certified translation in either language.
  • Patent applications are subject to substantive examination, while utility model applications need only be novel and industrial applicable. Substantive examination must be requested within 36 months from the application date.
  • Like many countries, the following inventions are not eligible for protection in Myanmar:
    1. Discoveries, scientific theories, mathematic formulae
    2. Schemes, rules and regulations or methods relating to conducting businesses, performing purely mental acts or playing games
    3. Pure computer programs
    4. Biological production technologies mainly used in agriculture and animal farming
    5. Plants and animals found in nature except man-made microbiological organisms, DNA (including complementary DNA sequences), cells, cell lines, cell cultures and seeds
    6. Surgical, treatment or diagnostic methods applied to human and animal bodies
    7. Inventions related to objects known to the public or chemical products prescribed as necessary
    8. Inventions detrimental to public order
About the Authors

Karen Bentley

Principal, Melbourne, Singapore | BAppSc (Hons), PhD, MIP Law

Karen’s focus: biotechnology, food technology, pharmaceutical, agricultural and life sciences.

Learn more about Karen
About the Authors

Desmond Tan

Principal, Singapore | BEng (Hons)

Desmond’s focus: engineering, clean energy technology, computing and telecommunications, and medical technology.

Learn more about Desmond
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