The Committee expresses its appreciation to the Ministry of Agriculture (MOA) for its engagement with industry over the past year and its collaborative approach in optimizing regulatory management. Building on this cooperation, we offer several recommendations to support continued modernization by aligning Taiwan’s pesticide management framework with international standards and promoting a transparent, efficient, and sustainable agricultural production system.
The agrochemical industry continues to face several regulatory bottlenecks, including administrative delays in the approval of maximum residue limits (MRLs), and recent changes in pesticide registration procedures that have reduced regulatory predictability and slowed the introduction of new technologies. Addressing these challenges is essential to maintaining Taiwan’s agricultural productivity and competitiveness. Equally important is the need for predictable registration procedures. Aligning Taiwan’s data requirements with internationally recognized hazard- and risk-based assessment principles would encourage investment in next-generation crop protection products with improved efficiency and lower toxicity profiles, and better aligned with sustainability objectives.
At the same time, enhancing the digitalization of regulatory management could improve administrative regulatory efficiency. Adopting e-labeling would not only reduce unnecessary and operational burdens associated with physical labeling change and product recalls while lowering carbon emissions. Thorough digital labels could also enable real-time verification of product information, helping authorities and farmers identify illegal pesticides more effectively.
Stronger and more coordinated enforcement against counterfeit and illegal pesticide products remains necessary to protect Taiwan farmers’ safety, ensure fair market competition, and safeguard consumer confidence in the safety and integrity of Taiwan’s agricultural products.
By advancing these measures, the Committee seeks to close the gap between regulatory policy and practical implementation while supporting a resilient, innovative, and sustainable agricultural sector in Taiwan.
Suggestion 1: Reduce unnecessary relabeling require-ments and promote the adoption of e-labels for pesticide products to protect farmers and consumer safety.
The Committee welcomes the amendments to Article 3 of the Regulations Governing Pesticide Labeling Management announced on September 18, 2025, by the Animal and Plant Health Inspection Agency (APHIA) under the MOA.
The revised article relaxes the six-month deadline for label changes in cases involving updates to factory information, while reinforcing requirements for labeling accuracy and consistency with actual conditions. This adjustment is a pragmatic regulatory improvement that reduces unnecessary administrative burdens and maintains the integrity of labeling standards. The Committee looks forward to the effective implementation of the revised provision through supporting measures and administrative guidance.
To build on this progress and further balance farmer safety, consumer rights, and practical industry operations, the Committee makes the following recommendations:
1.1 Waive product recall requirements for labeling changes that do not affect safety or public interest. When labeling updates involve only administrative information and do not affect instructions for use, warning statements, or safety information, companies should not be required to conduct full product recalls or reprinting after a six-month grace period. Allowing exemptions in such cases would reduce unnecessary waste and administrative costs while maintaining protection for farmers and consumers.
1.2 Facilitate the adoption of an e-label system for pesticide products. Allowing the use of digital labels would improve access to product information, increase regulatory efficiency, and strengthen supply chain transparency. E-labels would allow farmers to obtain the most up-to-date product information while enabling license holders to update labeling information more quickly in line with international practices. Digital labeling systems could also incorporate QR-code verification tools to help identify counterfeit products and reduce the circulation of illegal pesticides.
In addition, replacing physical labels with digital systems would reduce paper use, printing emissions, and label waste, supporting Taiwan’s sustainability and circular economy objectives. Integration of e-label systems with agricultural management platforms, such as electronic pesticide records and pesticide application history tracking, could further strengthen regulatory oversight and administrative efficiency.
The Committee recommends that APHIA establish a regulatory framework and support measures to enable the adoption of e-labels while allowing exemptions from recall and reprinting requirements when labeling changes do not affect product safety. This approach would enhance flexibility and efficiency in Taiwan’s labeling management system, supporting regulatory modernization and strengthening Taiwan’s agricultural competitiveness.
Suggestion 2: Ensure consistent and predictable pesticide registration and review management.
This issue was first raised in the 2023 White Paper and has since been discussed on several occasions between the Committee and the MOA. However, the Ministry has officially convened only two meetings on this issue: the consultation meeting on improving review mechanisms for new pesticide registration in October 2023 and the Consultation Meeting on the Draft Amendments to the Pesticide Management Act and Related Subordinate Regulations in August 2025.
In raising the issue once again in last year’s White Paper, the Committee stated: “In many developed countries, the information and standards required for pesticide management are clearly defined through laws, regulations, or published technical specifications, providing industry with a transparent and predictable compliance framework. In Taiwan, however, the absence of a consolidated and consistently published set of standards has resulted in persistent uncertainty for registrants.” It noted that “as a result, companies continue to operate without a stable regulatory reference, hindering planning and investment.”
Although the MOA responded in 2024 that revised regulations to remedy the problem would be completed before the end of that year, and repeated the pledge in 2025, the necessary revisions have yet to be finalized. Among the problems to be addressed is that the administrative and technical agencies under the MOA have not been applying a consistent interpretation of the data requirements for pesticide registration. As a result, the registration process lacks predictability. After initial submission, applicants are frequently required to provide repeated clarifications and supplementary submissions or incur additional investment to conduct tests. This wasteful situation creates uncertainty, increases compliance costs, and significantly delays the registration and market entry of new pesticide products.
To improve efficiency, the MOA in 2009 introduced a group registration system allowing data generated from trials on representative crops to be extended to similar crops or use against related pests. This approach was intended to address gaps in pesticide availability for minor crops and secondary pests, while supporting traceability and the principle of compliant pesticide use based on the approved application scope specified on pesticide labels.
In practice, however, current review procedures no longer reflect the original intent of the system. Even when applications fall within the scope of grouped registration, applicants are often required to submit additional field trial data, including studies on efficacy, phytotoxicity, and residue trials. The current framework has reverted to a pre-2009 model of single-crop, single-pest registration. Companies must conduct extensive additional trials to support expanded uses, significantly increasing time and financial burdens. At the same time, applicants are not granted a corresponding period of data protection for these additional studies. This imbalance reduces incentives for investment in expanded registrations and limits the availability of pesticide solutions for farmers, ultimately affecting the competitiveness of Taiwan’s agricultural sector.
The Committee recommends that the MOA:
2.1 Align pesticide data requirements with international hazard- and risk-based assessment principles. Data requirements under the “Guidelines for the Physicochemical and Toxicological Studies of Agro-Pesticides” (Article 3, Annexes 1 and 2) should be harmonized with international practices by allowing primary reliance on overseas test reports, rather than requiring additional local tests even when there are no domestic testing institutions able to conduct them. The current situation creates practical implementation difficulties and delays product registration.
2.2 Complete revisions to pesticide testing and registration regulations within one year. This should include revisions to the “Guidelines for Physicochemical and Toxicological Studies of Agro-Pesticides” and regulatory provisions governing grouped crops or pest species, representative use scopes, and implementation methods for extended uses under Article 4, Paragraph 1, Subparagraph 2 of the Guidelines for Pesticide Field Trials. Until these revisions are completed, applicants should not be required to submit data beyond what is required under existing regulations.
2.3 Provide data protection for additional trial data submitted to support extended-use registrations. When applicants are required to submit additional field trial data to support expanded uses, they should receive a corresponding period of data protection to prevent other parties from relying on that data. This structure would safeguard intellectual property and maintain incentives for continued investment in research and development.
2.4 Promote minor-crop registrations through flexible acceptance of scientifically valid trial data. Allowing the use of internal trial data that may not fully meet the formal requirements of the guidelines for pesticide field trials, but still demonstrate scientific validity, would increase industry willingness to pursue registrations and help address pesticide use gaps faced by farmers.
Suggestion 3: Optimize the review procedures for pesticide MRLs.
The Committee extends its appreciation to APHIA and the Agricultural Chemicals Research Institute under the MOA for their continued cooperation. In 2025, the Pesticide Review Committee convened monthly and worked to conclude application reviews within the same month. The Committee also acknowledges the efforts of the Taiwan Food and Drug Administration (TFDA) to improve transparency by regularly updating the status of pesticide MRL applications through the meeting minutes of the Food Sanitation, Safety, and Nutrition Advisory Committee.
Despite these improvements, delays remain in the overall review and approval process. In 2024 and 2025, the time taken by APHIA to forward approved cases to the TFDA frequently exceeded 60 days, compared with the originally planned 30-day timeframe. In addition, MRL review announcements were issued only twice in 2025, on March 11 and November 26. As multiple advisory committee review outcomes were consolidated into a single announcement, some cases took nearly one year to go from advisory committee review to official publication.
The establishment of pesticide MRLs is closely linked to national food security, the diversification of food import sources, and the introduction of high-efficiency, low-toxicity pesticides. The Committee therefore respectfully recommends that the MOA, in coordination with relevant agencies under the Ministry of Health and Welfare, continue to enhance the MRL review framework.
In particular, efforts should focus on strengthening alignment with international standards, improving review efficiency, and enhancing the transparency of decision-making processes. Advancing these measures would support timely access to safe agricultural inputs while safeguarding public health and food safety.
The Committee recommends that authorities prioritize the following actions:
3.1 Ensure that MRL cases approved by the advisory committee are submitted to the TFDA within 30 days. The MOA should strengthen internal coordination and administrative procedures to ensure timely case forwarding in line with the original review timeline.
3.2 Issue pesticide MRL announcements on a quarterly basis in accordance with advisory committee outcomes. Regular publication aligned with the meeting results of the Food Sanitation, Safety, and Nutrition Advisory Committee would improve transparency and reduce delays between review completion and official announcement.
Suggestion 4: Strengthen monitoring and enforcement against illegal pesticides to safeguard food safety and protect intellectual property rights.
The proliferation of illegal pesticides, including counterfeit and substandard products, continues to disrupt agricultural production and market order in Taiwan. These products are increasingly distributed through diverse and less regulated channels, further complicating detection and enforcement. From an economic perspective, illegal pesticides create unfair competition through lower pricing and informal distribution practices, eroding the market share and intellectual property of companies that have invested in research and development.
In some cases, counterfeit versions of innovative pesticide products have entered the market before the original products have received regulatory approval. This situation undermines the integrity of the registration system and weakens incentives for industry investment. If such practices persist, they may discourage the introduction of new technologies in Taiwan by international agrochemical companies and increase the risk of unauthorized use during the registration period.
Illegal pesticide products also pose significant risks to food safety and environmental sustainability. Because these products may contain unknown or unverified ingredients and have not undergone proper toxicological or environmental assessments, their use can result in excessive residues, soil degradation, and potential contamination. Detection of illegal pesticide residues in agricultural products may trigger trade restrictions and damage the international reputation and export competitiveness of Taiwan’s agricultural sector.
The Committee respectfully recommends the following actions:
4.1 Strengthen residue testing and enforcement mechanisms for unregistered pesticides. For pesticides not yet registered in Taiwan but already commercially available overseas, the MOA should enhance residue testing at major domestic fruit and vegetable wholesale markets and establish clear and enforceable penalties. Doing so would address the current gap in enforcement, under which residues of unregistered pesticides may go undetected or cannot be effectively penalized.
4.2 Strengthen source investigation and enforcement against illegal pesticides. The government should establish a dedicated enforcement mechanism to investigate the production and distribution of illegal pesticides. Regular training and policy guidance should be provided to police, prosecutors, investigators, and judicial personnel to strengthen understanding of the risks posed by counterfeit and substandard products. Enhanced investigative capacity and stronger source control would help curb the circulation of illegal pesticides and safeguard food safety.
委員會感謝農業部(MOA)過去一年來積極參與業界溝通並協助優化法規管理。基於此合作基礎,希冀能藉由以下建議促使台灣農藥管理框架能與國際標準接軌,並推動透明、高效且永續的農業生產系統,用以支持台灣農業的持續現代化發展。
當前農化產業仍面臨若干法規面向瓶頸,包括農藥殘留容許量(MRL)的審查行政延宕,以及近期農藥登記制度調整亦降低法規可預測性,進而延遲新技術及創新產品的引進。因此,解決這些挑戰對於維持台灣的農業生產力與競爭力至關重要。同樣重要的是建立具可預測性的登記查驗程序,且台灣之登記資料要求應與國際公認的「危害風險評估原則」一致,方能鼓勵業界引進高效、低毒且更符合永續發展目標的新一代作物保護產品。
與此同時,提升法規管理數位化亦有助於改善行政執行效率。導入「電子標示」(e-labeling)制度,不僅可以減少實體標籤及產品回收所衍生的非必要行政及營運負擔,亦有助於降低環境碳排放。透過數位化標籤,亦能實現產品資訊的即時確認,協助主管機關與農民更有效地識別非法農藥產品。
針對偽劣非法農藥產品,則應採取更強而有力的執法行動,以維護台灣農民用藥安全、確保市場公平競爭,以及保障消費者對台灣農產品安全性與完整性的信心。
透過推動上述措施,本委員會期盼能縮短法規政策與實際執行之間的落差,同時支持台灣農業朝向更具韌性、創新與永續的方向穩健發展。
建議一:標示變更內容若不影響農民用藥安全與消費者權益時,不須回收重製,並建議積極推行電子標示(e-labeling)
本委員會對農業部動植物防疫檢疫署(下稱防檢署)於 114 年 9 月 18 日公告之《農藥標示管理辦法》修正草案表示高度肯定。該草案第三條已明確放寬「工廠資訊變更」不受六個月標示變更期限之限制。此修正強化了「記載內容與事實相符」的定義,確保標示資訊真實、正確。委員會對此方向務實管理、降低行政負擔的修正方向表示肯定與支持,並期待後續能進一步落實於相關配套措施中。
建議:
為兼顧農民用藥安全、消費者權益與產業實務操作,建議如下:
1.1 若標示變更僅涉及行政資訊,且內容不影響公眾權益與農友合規用藥,應免除回收重製義務
例如僅為行政資訊調整、無涉及使用方法、警語或安全性資訊者,不應要求業者進行成本高、耗時長的全面回收重印,以降低不必要的浪費並促進產業效率。
1.2 建議主管機關積極推動 電子標示(e-labeling)制度
推動電子化標示將具備以下優勢:
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- 農民更便捷、快速取得最新且正確的產品資訊,並提供透明化的產品資料查詢管道。
- 與國際做法接軌,提升管理效能及資訊即時性。
- 降低不法與偽劣產品風險 。QR code 可結合驗證功能,使用者可即時掃描查驗是否為正品。有效減少偽造標籤與非法農藥流通,有助保護品牌與消費者安全。
- 落實永續與 ESG 目標,大幅降低紙張使用與印刷排放 、減少標籤浪費、降低碳足跡,符合循環經濟原則。
- 推動循環經濟與智慧農業,e-labeling 可讓資料與農業管理系統深度整合(如農藥電子紀錄、施藥歷史追蹤),強化行政管理效能。
推動 e-labeling 具有提升資訊透明度、保障農民與消費者安全、降低產業負擔、強化行政效率及與國際接軌等明顯優勢。
因此,建議主管機關積極建立 e-labeling 法規框架與配套措施,同步允許對不影響安全性的標示變更,免除回收重印義務,使我國標示管理更具彈性與效能。
建議二:一致且可預測性的農藥登記及審查管理
此議題於2023年提出並多次拜會農業部,此期間僅於2023年10月召開「精進新農藥登記相關審查機制座談會」及2025年8月召開《農藥管理法》及相關子法修正草案研商會議。本委員會在去年的白皮書中亦再次提出該問題,指出:「在許多已開發國家,農藥登記所需的資訊和標準均皆詳細明定於法規或公告相關說明以利遵循,為產業提供透明且可預測的法規框架。然而,在台灣由於缺乏統一且持續更新的標準,導致申請登記廠商持續面臨不確定性。因此,廠商在缺乏明確標準下影響投資意願及業務規劃。
儘管農業部於2024及2025年白皮書卻分別回應將於該年年底前完成「農藥理化性及毒理試驗準則」修正法制作業,但至今仍未完成。究其主因係農業部轄下管理機關及技術機關對於資料要求仍無共識,導致業者在法規不明確的情形下,辦理農藥登記作業受阻,來回釐清補件,或額外增加投資進行試驗,已嚴重延誤創新藥劑無法登記上市。
另外,民國 98 年即已法制化「群組化」登記制度,初衷為解決少量作物或是次要害物的用藥缺口,並透過試驗資料延伸利用,同時為因應產銷履歷制度與維持「農藥標示指導用藥之制度」,然執行至今逾16年後,現行審查已無法以法規要求使用既有代表作物資料辦理登記,轉而需額外繳交欲延伸使用範圍登記作物所費不貲之藥效、藥害或是殘留等各項田間試驗報告。此種實務運作幾乎已使制度退回民國98年以前「單一作物單一害物之登記制度」,業者不僅須負擔高昂的延伸登記田間試驗費用,卻也無法享有對應的資料保護期,此種制度性的倒退已嚴重削弱產業的投資意願與農業競爭力 。
建請主管機關:
2.1 「農藥理化性及毒理試驗準則」(第三條附件一及二)之資料要求應與國際接軌並考量以危害風險評判做為評估原則,以國外所製備之各項試驗報告審理為主,而非額外要求執行無試驗單位可執行之本地試驗,將造成實務執行困難並延遲產品登記。
2.2 一年內完成「農藥理化性及毒理試驗準則」(第三條附件一及二)、「田間試驗準則」及「田間試驗準則第4條第1項第2款延伸使用範圍之群組化作物或有害生物種類、代表性使用範圍及其實施方式之法制作業」,在相關法制作業完成前,不應強制要求補充法規要求外之各項試驗資料。
2.3 申請人所繳交之各項試驗資料皆有其智財權,辦理延伸登記使用如有繳交代表作物外之試驗資料,該登記案應給予資料保護期,以保障業者研發投入之權益。
2.4 為鼓勵廠商辦理少量作物登記,請研議彈性採認雖未完全符合田間試驗準則要求但具備科學評估價值之內部試驗資料,以增加產業投資意願並解決農民用藥缺口。
建議三:優化農藥殘留容許量審查程序
委員會感謝農業部防檢署及農業部藥物試驗所(以下簡稱農藥所)密切合作,農藥技術諮議會(以下簡稱農藥諮議會)於114年度每月均有開會審查,並盡可能將業者申請案於當月結案。亦感謝食藥署即時更新由農業部向其送件之農藥最大殘留容許量申請案件之辦理情況,並於「食品衛生安全與營養諮議會」會議紀錄中呈現當次審查案件,提升案件進度透明度。
然據本委員會觀察到,防檢署於113、114年通過諮議會後提送食藥署之時程,多數案件超過60天,較防檢署先前規劃之30天超出許多。關於農藥殘留容許量,分別於114年03月11日及114年11月26日公告兩次,但依據114年「食品衛生安全與營養諮議會」會議紀錄,其中第二至五次會議皆有審查殘留容許量,因合併數次會議結果併案預告,導致某些案件自諮議會審查至正式公告須近一年。
委員會建議主管機關採取以下措施:
3.1 建議農業部加速行政效率,使通過諮議會之案件可於30日送達食藥署。
3.2 建議食藥署依「食品衛生安全與營養諮議會」開會結果每季辦理預公告。
農藥殘留容許量之訂定,攸關國民糧食安全、食品進口來源之多元化及新型高效低毒農藥引進之可行性。爰此,敬請農業部及衛福部所屬相關機關持續檢視並優化審查制度與資訊揭露機制,積極推動農藥殘留容許量(MRL)國際調和,以確保與國際標準接軌,提升審查效率與透明度,並共同維護國民健康及食品安全。
建議四:全面強化非法農藥殘留監測與建立查緝機制,以維護食安誠信市場並保障智慧財產權
當前非法農藥(偽劣藥)之氾濫,已跨越原來的農藥銷售渠道,除了衝擊農業生態及市場秩序。在經濟層面,非法農藥藉由高渠道利潤和低價進行惡性競爭,侵蝕合法企業投入鉅額研發之智慧財產和市場佔有率。尤有甚者,部分處於登記審查階段之創新藥劑,在合法上市前,市場竟以偽農藥型態進行銷售;此現象若持續存在,將嚴重打擊國際農化企業在台投資之意願,導致增加登記審查期間遭非法使用之風險,造成食安問題。
偽劣農藥因成分來源與含量不明,缺乏正確的使用指引,亦未經毒理試驗及環境安全評估,極易造成作物殘留、土壤不可逆損害及潛在污染。一旦農產品檢出非法農藥殘留,將直接觸發國際貿易壁壘,重創國家農業品牌之國際聲譽與外銷競爭力。
為維護產業健全發展並守護食安,建議主管機關應採取下列措施:
4.1 落實殘留檢驗與處罰機制: 針對尚未在台灣完成登記之農藥,政府應在其於國外上市後,即同步強化國內各大果菜批發市場的末端殘留檢驗機制,並明確建立相關罰則。此舉可有效彌補未登記農藥殘留不易被偵測或難以有效裁罰之執法缺口。
4.2 落實源頭查緝: 建議成立專責的非法農藥查緝警政單位,並由主管機關定期對檢警調及司法機關進行偽劣農藥相關教育訓練及政策溝通,使執法人員充分理解非法農藥帶來的食品安全、環境永續與產業經濟之重大影響。透過積極主動的查緝與源頭遏止,方能有效防堵非法農藥流通,確保國人食安。

