Answer: The process generally covers six stages: importer eligibility and product classification; formula and safety review; applicable product permits; Chinese labels and claims; customs clearance, import inspection and any required quarantine; and ongoing compliance.

Evershine recommendation: Complete classification and formula screening before shipment so that missing evidence, label changes and permit requirements can be addressed early.

Official references (Chinese): Act Governing Food Safety and Sanitation · Food product registration and permit management rules · Inspection of imported foods and related products · TFDA import-inspection FAQ · Exporter/importer registration

Q02. Does incorporating a Taiwanese company authorize food imports and sales?

Answer: Incorporation alone is insufficient. Check applicable exporter/importer registration and food-business registration, including the actual import and sales activities. The product must also meet ingredient, permit, labelling and shipment-inspection requirements.

Business registration, food-business registration and product authorization are separate compliance steps.

Official references (Chinese): Act Governing Food Safety and Sanitation · Exporter/importer registration · Food-business registration portal

Q03. Does every imported food need a prior TFDA product permit?

Answer: No. Prior product registration depends on the legal category. Imported food tablets/capsules, statutory health foods, infant/follow-up formula and foods for special medical purposes require assessment under their respective systems.

A product that does not require a prior permit must still comply with food safety, labelling and applicable import inspection rules. Products classified as medicines follow the pharmaceutical framework.

Official references (Chinese): Act Governing Food Safety and Sanitation · Food product registration and permit management rules · Registration notice for imported food tablets and capsules · Health Food Governing Act

Ingredients and Food Safety

Q04. What information should be obtained from the overseas manufacturer?

Answer: Request the quantitative formula, recommended daily intake, manufacturing process, specifications, origin, manufacturer details and relevant test reports. Break down compound ingredients, additive mixtures, capsule shells and coatings.

Identify botanical species, plant parts and processing methods, as well as animal or microbial sources where relevant. This is a pre-screening recommendation; mandatory filing documents depend on the product category and current application requirements.

Official references (Chinese): TFDA applicant self-check form for imported tablets/capsules · Emerging food material safety assessment principles

Q05. Does a restricted ingredient automatically make a product prohibited?

Answer: Not necessarily. Restrictions may concern the source, permitted part, process, daily intake, food category or warnings. Assess compliance with all applicable conditions before determining whether the product can proceed.

An outright prohibition is different from permission subject to conditions.

Official references (Chinese): Act Governing Food Safety and Sanitation · Government guidance on the food-material database · TFDA food-material database

Q06. Is an ingredient prohibited if it is absent from TFDA’s food-material database?

Answer: Absence alone does not establish prohibition, because the database is not an exhaustive list of traditional food materials. It also does not establish permission.

Review the identity, consumption history, process and safety evidence, and seek clarification where needed. Ordinary food materials and food additives are governed differently.

Official references (Chinese): Government guidance on the food-material database · TFDA food-material database · Emerging food material safety assessment principles · Food additive scope, limits and specifications

Q07. How should an emerging food material be assessed?

Answer: First determine whether the material falls within TFDA’s emerging-food-material safety assessment principles. Limited evidence of safe consumption or changes arising from breeding or processing may trigger further assessment.

The principles issued on 27 January 2026 provide for a classification questionnaire and supporting evidence, followed by safety data as required by the classification. Do not assume that every material requires the same test package.

Official references (Chinese): Emerging food material safety assessment principles · TFDA notice issuing emerging-food-material principles

Q08. Can an additive permitted overseas be used in Taiwan?

Answer: Foreign permission does not automatically establish compliance in Taiwan. Check the permitted identity, purpose, food category, level and specification under Taiwan’s additive standard, including category-specific rules for flavourings.

Check effective dates as well. The May 2025 amendment includes provisions already in force and others effective on 1 July 2027.

Official references (Chinese): Food additive scope, limits and specifications

Q09. Does Taiwan apply zero tolerance to all pesticide residues?

Answer: The legal concepts are residue limits and “not detected,” subject to the standard’s scope and exceptions. Article 3 applies to foods other than animal products: listed residues must meet the limits, while unlisted residues generally must not be detected. Article 4 provides exemptions, and banned pesticides have separate rules.

Assessment requires the correct food category, pesticide/residue definition, tables and analytical method.

Official references (Chinese): Pesticide residue limits

Q10. How are veterinary-drug residues in meat or dairy assessed?

Answer: Match the drug, species, tissue or product, and marker residue to Taiwan’s veterinary-drug residue standard. Listed items must meet the applicable limits; unlisted drug items must not be detected.

Some entries apply only to imported meat. Assess dairy against the correct entries rather than treating every veterinary-drug residue as categorically prohibited.

Official references (Chinese): Veterinary-drug residue limits

Q11. Is a COA sufficient to establish that a food can be imported?

Answer: No. A Certificate of Analysis is supporting evidence. Review the test scope, methods, batch, applicable limits and specifications, as well as the legality of the ingredients.

Apply contaminant and toxin limits to the correct food category, including relevant amendments effective January 2026. Microbiological and other risks may need separate assessment. Contaminant limits do not authorize intentional adulteration. Passing tests does not replace permits, labelling compliance or import inspection.

Official references (Chinese): Act Governing Food Safety and Sanitation · TFDA applicant self-check form for imported tablets/capsules · Food contaminant and toxin standards · Inspection of imported foods and related products

Product Registration and Permits

Q12. Do imported food tablets and capsules require prior registration?

Answer: Commercial imports of food tablets and capsules generally require prior registration and a permit under the applicable notice. Special forms require separate classification assessment. A product permit does not replace shipment-level import inspection.

For 2026, TFDA delegated the relevant reviews to the Taiwan CAS development association. Use the official contacts and forms applicable when filing.

Official references (Chinese): Registration notice for imported food tablets and capsules · Food product registration and permit management rules · TFDA 2026 delegation of tablet/capsule reviews · Inspection of imported foods and related products

Q13. How do supplements, food tablets/capsules and statutory health foods differ?

Answer: “Supplement” is a commercial description and does not determine the Taiwanese legal category. “Health food” is a statutory category subject to authorization and health-effect controls.

An imported tablet/capsule food permit is not an authorization for statutory health-food claims. Marketing a product as a health food or making claims governed by that authorization system requires compliance with the Health Food Governing Act.

Official references (Chinese): Health Food Governing Act · Registration notice for imported food tablets and capsules · Act Governing Food Safety and Sanitation

Q14. Can effervescent tablets automatically be treated as exempt from registration?

Answer: Do not determine exemption from the product name alone. Review the complete formula, directions for use, physical form and product positioning to establish its classification and applicable registration requirements. This FAQ does not make a blanket exemption determination for effervescent tablets.

Even if the ordinary imported tablet/capsule registration requirement does not apply to a particular product, ingredient, labelling, inspection and other applicable permit requirements remain relevant.

Official references (Chinese): Food product registration and permit management rules · Registration notice for imported food tablets and capsules · TFDA tablet/capsule application forms

Q15. What documents are needed, and is a free-sale certificate always mandatory?

Answer: Core documents generally include the application, manufacturer-issued quantitative formula, official evidence of lawful manufacturing, applicant business registration, samples or required photographs, and product particulars. Contract manufacturing, particular ingredients or other circumstances can require additional evidence. Use the current application and self-check form for the complete requirements.

A separate free-sale certificate should not be described as universally mandatory. Its acceptability depends on the issuer, content and document conditions, not its title alone.

Official references (Chinese): TFDA applicant self-check form for imported tablets/capsules · Food product registration and permit management rules · TFDA tablet/capsule application forms · Supporting tablet/capsule registration requirements

Chinese Labels and Advertising Claims

Q16. What information must appear on a Chinese food label?

Answer: Packaged foods generally require Chinese labelling under Article 22 and related notices: product name, ingredients, additives, net contents, manufacturer or responsible domestic business details, origin, expiration date, nutrition, GMO information and other applicable particulars.

Ingredients in mixtures generally appear in descending order of quantity. Check product-specific allergen statements, warnings and exemptions. A statement such as “shelf life: 24 months” alone does not replace the expiration date.

Official references (Chinese): Act Governing Food Safety and Sanitation

Q17. Can overseas claims simply be translated for use in Taiwan?

Answer: Review them first. A claim permitted overseas may not comply in Taiwan. Assess Chinese and retained foreign-language labels, websites, advertisements and other sales materials against the Taiwanese product classification.

Food claims must not be false, exaggerated or misleading, or assert medical efficacy. Statutory health-food claims must also comply with the relevant authorization and controls.

Official references (Chinese): Act Governing Food Safety and Sanitation · Health Food Governing Act

Customs, Border Inspection and Quarantine

Q18. How do I determine inspection requirements, filing time and documents?

Answer: Check the customs-assigned CCC classification and import requirements. TFDA identifies products subject to relevant codes such as F01, F02 and 508 as requiring import inspection under the applicable rules.

Apply within 15 days before arrival or after arrival. Core documents include the inspection application, product data sheet, import declaration copy and designated evidence. Prepare invoices, packing lists and bills of lading for customs, with product permits or official certificates where applicable.

Official references (Chinese): TFDA import-inspection FAQ · Inspection of imported foods and related products

Q19. Will every shipment be sampled for laboratory testing?

Answer: Not necessarily. The authority applies the relevant inspection method according to risk and regulatory requirements. An obligation to apply for import inspection does not mean that every shipment will undergo laboratory testing.

A shipment not selected for testing remains subject to food safety obligations. A permit or an earlier compliant shipment does not waive requirements for future consignments.

Official references (Chinese): Inspection of imported foods and related products · Act Governing Food Safety and Sanitation

Q20. Can food be sold immediately after conditional early release?

Answer: Check the basis of the release. Conditional early release generally allows custody under specified conditions; it does not itself establish completion of inspection or unrestricted permission to sell or use the goods.

Confirm completion of TFDA inspection, customs clearance, applicable quarantine and all other market-entry requirements before sale.

Official references (Chinese): Act Governing Food Safety and Sanitation · Inspection of imported foods and related products

Q21. Does TFDA clearance remove animal or plant quarantine requirements?

Answer: No blanket exemption follows from TFDA clearance. Animal, plant and derived products may face separate quarantine requirements linked to origin, species, processing, establishment or official certification.

Determine the requirements for the actual product. Food inspection and animal/plant quarantine are separate procedures.

Official references (Chinese): Animal and animal-product quarantine conditions · Plant quarantine requirements · TFDA import-inspection FAQ

Q22. Can personal-use imports be used for a small market test involving sales?

Answer: Personal-use exemptions cannot be used as authorization for commercial resale. They are subject to purpose and quantity/value conditions.

Commercial samples, exhibition goods and other non-sale uses may have separate application procedures and restrictions. A trial involving sales should be planned as a commercial activity.

Official references (Chinese): TFDA import-inspection FAQ · Act Governing Food Safety and Sanitation

Ongoing Compliance and Project Planning

Q23. What ongoing obligations apply after the product enters the market?

Answer: Maintain source, batch, distribution and supporting records, with applicable traceability and recall arrangements. Confirm food-business registration annually and generally apply to update registered details within 30 days of a change.

Manage permit validity and required changes, and check applicable product liability insurance. Reassess formula, manufacturer, label and origin changes.

Official references (Chinese): Act Governing Food Safety and Sanitation · Food product registration and permit management rules · Food-business registration regulations · Food-business product liability insurance requirements

Q24. Can a fixed timeline and budget be given at the outset?

Answer: A reliable estimate requires classification, formula assessment, a review of document completeness and identification of permits or additional studies. Ordinary food, imported tablets/capsules and statutory health foods should not share one assumed timeline or cost.

Evershine recommendation: Budget separately for pre-screening, permits, testing, labels and shipment clearance. Distinguish official charges, third-party costs and advisory fees, and allow for supplementation and studies. Confirm amounts and timing for the actual case.

Official references (Chinese): Food product registration and permit management rules · TFDA applicant self-check form for imported tablets/capsules · Inspection of imported foods and related products · Health Food Governing Act

Q25. What is the best starting point for a Taiwan market-entry project?

Answer: Begin with a regulatory pre-screen: identify commercial objectives and intended claims, then review the quantitative formula, directions for use, process, sources and labels. Map feasible routes, evidence gaps and filing sequence.

Evershine recommendation: Where statutory health-food claims are unnecessary, first assess whether the ordinary-food route is feasible. Where those claims are needed, assess health-food authorization. The ordinary-food route may still require tablet/capsule registration or ingredient safety assessment; it does not guarantee immediate import.

Provide the formula, labels, manufacturer details and proposed sales model so the Evershine team can assess the appropriate scope of assistance.

Official references (Chinese): Act Governing Food Safety and Sanitation · Registration notice for imported food tablets and capsules · Emerging food material safety assessment principles · Health Food Governing Act

What are procedures when importing a foreign food into Taiwan?

Step 1. Composition Review

Check whether any ingredient is listed as prohibited or restricted by the Taiwan Food and Drug Administration (TFDA).
If prohibited, the product cannot be imported.
Required Documents:

Full ingredient list (with percentage)
Certificate of Analysis (COA)
Product specification sheet

Step 2. Special Forms (Tablet / Capsule) – Pre-Market Approval

If the product is in tablet or capsule form (often considered close to dietary supplements), you must apply for TFDA pre-market approval before import.
Required Documents:

Application form to TFDA
Ingredient safety data
Free Sale Certificate from country of origin
Manufacturing license of factory

Step 3. Food Labeling & Marking

Prepare a Chinese food label compliant with Taiwan’s Food Labeling Act.
Labels must include:

Product name
Ingredient list
Net weight/volume
Expiry date / shelf life
Importer’s name, address, and phone number (must be Taiwan registered entity)
Country of origin
Nutrition facts (if required)

Step 4. Import Declaration & Border Inspection

File an import declaration with Taiwan Customs, and submit the product to TFDA border inspection. If passed, TFDA issues a release notice, and goods can enter the Taiwan market.
Required Documents:

Import declaration form
Invoice, packing list, bill of lading
TFDA pre-approval (if applicable)
Chinese label sample

Summary Table

Step	English	中文	Key Notes
1	Composition Review	成分審查	Check TFDA prohibited list
2	TFDA Approval (if capsule/tablet)	膠囊/錠劑需申請 TFDA 核准	Applies only for supplements-type forms
3	Food Labeling	食品中文標示	Must comply with TFDA labeling rules
4	Import & Border Inspection	進口報關與邊境查驗	Customs + TFDA clearance

Official References

TFDA – Food Safety and Inspection: Food Import Regulations (中文)

Taiwan Food and Drug Administration (TFDA): https://www.fda.gov.tw/ENG/

What category of composition are prohibited or restricted ?

Check whether any ingredient is listed as prohibited or restricted by the Taiwan Food and Drug Administration (TFDA).
If prohibited or restricted, the product cannot be imported.

1) Food additives

Only additives listed in TFDA’s “Standards for Specification, Scope of Application and Limitation of Food Additives” may be used, and only in the specified foods and at/under the stated limits. If an additive is not listed, it is prohibited. 食品藥物管理署

Where to check
TFDA English law page & Appendix tables（英/中）：食品藥物管理署+1

2) Pesticide residues (MRLs)

Foods must meet TFDA “Standards for Pesticide Residue Limits in Foods.” Taiwan uses a positive list; if a pesticide/commodity MRL is not listed, it is not allowed (zero-tolerance by default). 食品藥物管理署+1

Where to check
TFDA English law page

3) Veterinary drug residues

Foods must comply with “Standards for Veterinary Drug Residue Limits in Foods.” Drugs not listed shall not be detected; listed drugs must not exceed the given limits. 食品藥物管理署+1

Where to check
TFDA English law page（英）與PDF（中）：食品藥物管理署+1

4) Heavy metals, mycotoxins & other contaminants

Foods must meet TFDA “Sanitation Standard for Contaminants and Toxins in Food.” Anything above the maximum levels is prohibited; limits have been recently tightened for some categories (e.g., infant/young child foods, offal, nuts/oils). 全國法規資料庫+2USDA Apps+2

Where to check
TFDA English index（英）與合併標準解讀：食品藥物管理署+1

5) Form-factor & import inspection triggers

All imported food, food additives, utensils/packaging, cleansers are subject to border inspection under TFDA’s import inspection regulations. Tablet/capsule “food” often faces pre-market scrutiny and must still comply with the above substance standards. 食品藥物管理署

Practical “Prohibited/Restricted” examples

Additives not listed in TFDA additive standard → prohibited. 食品藥物管理署
Pesticide residues beyond TFDA MRLs or not listed at all → not allowed. 食品藥物管理署+1
Veterinary drugs not listed (detectable) or exceeding limits → not allowed. 食品藥物管理署+1
Contaminants (e.g., lead, cadmium, aflatoxins) exceeding TFDA maximum levels → not allowed (note: several heavy-metal limits were tightened effective 2024/7/1). USDA Apps+1
Melamine and veterinary drug residues in milk specifically flagged as prohibited in dairy standards (illustrative historical rule). USDA Apps

How to use this in compliance reviews

List every ingredient/additive with CAS No. and inclusion rate.

Verify each additive against TFDA’s additive Appendix (if not listed → prohibited).
For agricultural/animal ingredients, verify pesticide/veterinary-drug limits and test reports.
Check contaminant limits relevant to the food category.
Keep records for TFDA border inspection.

Official references

Additives ：TFDA “Standards for Specification, Scope, Application and Limitation of Food Additives” （未列名不得用）食品藥物管理署
Pesticide MRLs：TFDA “Standards for Pesticide Residue Limits in Foods”（採正面表列）食品藥物管理署+1
Veterinary drugs：TFDA “Standards for Veterinary Drug Residue Limits in Foods”（未列名不得檢出）食品藥物管理署+1
Contaminants/Toxins：TFDA index + WTO/USDA通報（2024/7/1修正）食品藥物管理署+1
Import inspection：TFDA “Regulations of Inspection of Imported Foods and Related Products” 食品藥物管理署

My take

Taiwan is strictly positive-list for additives and residues. If your ingredient/additive isn’t explicitly listed with a permitted use, assume “no.” This is the safest default for client advice. 食品藥物管理署+2USDA Apps+2
For risk control, build a pre-screen matrix (ingredient ↔ TFDA table entry ↔ allowable food type ↔ max level ↔ COA/test report). I can draft this matrix (bilingual) if you want.

Taiwan food import: source URLs

Checked: 2026-10-03
N01 Non-official Article https://www.wfoe-accounting.com/what-are-procedures-when-impwhat-procedures-when-importing-foreign-food-into-taiwan-ct

Original URLs: exact tracking parameters retained

O01 Official TFDA英文首頁 https://www.fda.gov.tw/ENG/
O02 Official 食品添加物標準英文頁 https://www.fda.gov.tw/ENG/lawContent.aspx?cid=16&id=308&utm_source=chatgpt.com
O03 Official 農藥殘留標準英文頁 https://www.fda.gov.tw/eng/lawContent.aspx?cid=16&id=304&utm_source=chatgpt.com
O04 Official 動物用藥殘留標準英文頁 https://www.fda.gov.tw/ENG/lawContent.aspx?cid=16&id=306&utm_source=chatgpt.com
O05 Official 污染物及毒素標準英文頁 https://law.moj.gov.tw/ENG/LawClass/LawAll.aspx?pcode=L0040138&utm_source=chatgpt.com
O06 Official TFDA英文法規分類清單第7頁 https://www.fda.gov.tw/ENG/law.aspx?cid=16&cr=89351&p=7&utm_source=chatgpt.com
O07 Official 輸入查驗辦法英文頁 https://www.fda.gov.tw/ENG/lawContent.aspx?cid=16&id=1356&utm_source=chatgpt.com
O08 Official Taiwan Publishes Draft Amendment for Toxins in Food Levels https://apps.fas.usda.gov/newgainapi/api/Report/DownloadReportByFileName?fileName=Taiwan+Publishes+Draft+Amendment+for+Toxins+in+Food+Levels_Taipei_Taiwan_TW2023-0052.pdf&utm_source=chatgpt.com
O09 Official Food and Agricultural Import Regulations and Standards—Narrative https://apps.fas.usda.gov/newgainapi/api/report/downloadreportbyfilename?filename=Food+and+Agricultural+Import+Regulations+and+Standards+-+Narrative_Taipei_Taiwan_12-16-2016.pdf&utm_source=chatgpt.com

Supplementary official sources

S01 Official 食品安全衛生管理法 https://laws.gov.taipei/Law/LawSearch/LawArticleContent/FL013890
S02 Official 食品與相關產品查驗登記及許可文件管理辦法 https://www.fda.gov.tw/tc/siteListContent.aspx?id=45742&sid=3903
S03 Official 輸入錠狀、膠囊狀食品應辦理查驗登記公告 https://www.fda.gov.tw/tc/includes/GetFile.ashx?id=f636697218764222903
S04 Official 輸入錠狀膠囊狀食品查驗登記—廠商自檢表 https://www.fda.gov.tw/tc/includes/GetFile.ashx?id=f638729701469194538&type=1
S05 Official 115年度輸入錠狀膠囊狀食品查驗登記委託審查公告 https://www.fda.gov.tw/tc/newsContent.aspx?cid=3&id=25873
S06 Official 新興食品原料安全性評估作業原則 https://www.fda.gov.tw/tc/includes/GetFile.ashx?id=f639051027182990730
S07 Official 食品原料整合查詢平台使用說明 https://www.ptshb.gov.tw/News_Content.aspx?n=4F335CEFBA319842&s=0495A28F0A19BCDD&sms=3AC5221F20283EEC
S08 Official 食品原料整合查詢平台 https://consumer.fda.gov.tw/Food/Material.aspx?nodeID=160
S09 Official 食品添加物使用範圍及限量暨規格標準 https://law.moj.gov.tw/LawClass/LawAll.aspx?pcode=L0040084
S10 Official 農藥殘留容許量標準 https://law.moj.gov.tw/LawClass/LawAll.aspx?pcode=L0040083
S11 Official 動物用藥殘留標準（94.04.15訂定） https://law.moj.gov.tw/LawClass/LawAll.aspx?pcode=L0040026
S12 Official 食品中污染物質及毒素衛生標準 https://law.moj.gov.tw/LawClass/LawAll.aspx?pcode=L0040138
S13 Official 食品及相關產品輸入查驗辦法 https://www.fda.gov.tw/tc/includes/GetFile.ashx?id=f638913659559818692
S14 Official 食品輸入查驗常見問答 https://www.fda.gov.tw/tc/faqContent.aspx?id=1114
S15 Official 出進口廠商登記流程 https://www.trade.gov.tw/ProcessList/ProcessList.aspx?nodeID=4365&pid=1
S16 Official 動物及畜產品輸入檢疫條件 https://www.aphia.gov.tw/ws.php?id=3535
S17 Official 植物檢疫相關輸入規定 https://www.aphia.gov.tw/ws.php?id=3600
S18 Official 非登不可食品業者登錄平台 https://fadenbook.fda.gov.tw/
S19 Official 食品業者登錄辦法 https://www.fda.gov.tw/tc/includes/getfile.ashx?id=f637237767035817959
S20 Official 食品業者投保產品責任保險規定 https://www.fda.gov.tw/tc/includes/GetFile.ashx?id=f637680900641721044
S21 Official 健康食品管理法 https://www.fda.gov.tw/tc/siteListContent.aspx?id=18087&sid=1758
S22 Official 輸入錠狀膠囊狀食品查驗登記Q&A（舊附件） https://www.fda.gov.tw/tc/includes/GetFile.ashx?id=f637575253224639681
S23 Official 輸入錠狀膠囊狀食品申辦資料目錄 https://www.fda.gov.tw/TC/siteList.aspx?sid=1651
S24 Official 新興食品原料安全性評估作業原則發布公告 https://www.fda.gov.tw/tc/newsContent.aspx?cid=3&id=31400
S25 Official 輸入錠狀膠囊狀食品查驗登記相關規定 https://www.fda.gov.tw/tc/includes/GetFile.ashx?id=f637196298242325942&type=1

Unavailable candidate attachments (not relied on as current text)

UNAVAILABLE Official 舊膠錠問答 https://www.fda.gov.tw/tc/includes/GetFile.ashx?id=f637575253224639681
UNAVAILABLE Official 舊膠錠申辦說明 https://www.fda.gov.tw/tc/includes/GetFile.ashx?cid=10698&id=f637196293634412499&type=2
UNAVAILABLE Official 配方相關候選附件 https://www.fda.gov.tw/tc/includes/GetFile.ashx?id=f639076283795757486&type=4
UNAVAILABLE Official 食品標示問答候選附件 https://www.fda.gov.tw/tc/includes/GetFile.ashx?cid=42306&id=f638745245032165502

Warning :

Contact Us

tpe2ww.food@evershinecpa.com.

You may also call in working hours (Taipei and China Time):
Director Jerry Chu, USA Graduate School Alumni and a well-English speaker
Mobile: +886-939-357-735
Tel No.: +886-2-2717-0515 ext. 103

Additional Information

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Evershine Potential Serviceable City (2 months preparatory period):
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Besides, Evershine is Taiwan local Partner of ADP Streamline ®.
(version: 2024/07)

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