SNQ Quality Mark

SNQ is built on evidence-based standards, setting trusted quality and safety benchmarks for healthcare, biomedical, health, and animal care services and products.

  • 9F, No. 508, Sec. 7, Zhongxiao E. Rd., Nangang Dist., Taipei City, Taiwan
  • +886 2 2655 7888
  • snq@snq.com.tw

About the National Quality Mark

  • Vision & Mission
  • Review Committee
  • Certification Schedule

Certification Methods

  • Medical Service
  • Biomedical Product
  • Health Product
  • Animal Care & Products

SNQ Certified

  • Certified Services & Products
  • Certified Organizations
  • Quality Award Winners

International Certification

  • ICHOM PROMs
  • NSF Certification

Quality Focus

  • Apply for Certification →
Organized by|Research Center for Biotechnology and Medicine PolicyOperated by|Kuanglu International Quality Standards Co., Ltd.© 2026 Kuanglu International Quality Standards Co., Ltd. All rights reserved.Privacy Policy
SNQ Quality Mark
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Application Regulations

Scope of Application

Applications must be submitted by a single institution for one service, technology, process, project or product.

Regulatory Compliance

Applications must comply with all relevant laws and regulations, and shall not involve false claims, infringement, counterfeiting, or violations of intellectual property rights.

Application Documents

All submitted documents and supporting reports must be true and accurate. Any falsification or misrepresentation will lead to disqualification or termination of certification, a three-year prohibition on re-application, and full legal liability borne by the applicant.

Data Handling

The certification body and review committee are obliged to maintain confidentiality of application materials. However, all submitted documents, attachments, and physical products will not be returned, regardless of review outcome.

Refund Policy

Once the review process has commenced, application fees are non-refundable, regardless of withdrawal or disqualification.

Mark Authorization

Certified items, upon receipt of official notification, are required to sign the "SNQ License Agreement" before being formally authorized to use the SNQ Mark and its related identifiers.

Nutritional & Health Supplements

Recognizing products that excel in health supplements, health foods, nutritional and special dietary foods, and functional health ingredients.

  1. Home
  2. Application
  3. Nutritional & Health Supplements

Overview

What is Evaluated:

Quality control and safety standards, manufacturing process audits, product efficacy, innovation, and market influence.

Who Can Apply:

Registered enterprises and institutions (including manufacturers, importers, and agents).

Why It Matters:

Strengthen consumer trust, promote scientific innovation, ensure product safety and quality, and expand domestic and international market influence.

Subcategories & Criteria

Eligibility:Distinctive dietary supplement products with validated health benefits, innovative formulations, or advanced production processes.
Evaluation Criteria & Weighting:
  1. Company Operation (10%)
  2. Review basic corporate information including company name, establishment date, person in charge of the company, capital, business scope, etc.
    Assess company vision, management team, workforce, organizational quality system, current business operations and overall organizational performance.
    Evaluate market strategy, positioning, scale of operations, sales achievements, market share, and competitiveness.
    Review social recognition and contributions to public welfare initiatives.
  3. Product Features (15%)
  4. Evaluate product uniqueness, innovative formulations, and differentiation in the market.
    Assess the criticality of applied technologies. Products developed through domestic research or those adopting outcomes from academic or research institutions should provide strengthened explanations to highlight their value.
    Review patent types, application countries, and acquisition status.
  5. Practical Impact (25%)
  6. Review active ingredients and concentrations. Applicants must specify the functional health claims of indicator ingredients and provide supporting test reports or certification documents.
    Evaluate intended use, consumption methods, and demonstrated health benefits.
    Assess verified data, clinical studies, and evidence supported by a literature review.
    Review the importance of domestic and international market, including sales data, import/export values, and growth potential. Applicants should provide sales revenue, import values, and export values from the most recent year.
  7. Quality Control (30%)
  8. a. List all active ingredients and additives.
    b. Provide raw material source documentation (e.g., COA) and quality acceptance reports for labeled ingredients.
    c. Demonstrate quality assurance measures to verify ingredient content (e.g., raw material dosage conversion, laboratory quantitative analysis).
    d. Submit proof of compliance with food registration or traceability systems required by authorities.
    a. Confirm manufacturing facilities comply with FSSC, ISO22000, or HACCP standards.
    b. QC Flow Chart: Applicants must provide detailed flow charts that illustrate:
    - Raw material sourcing
    - Production stages
    c. Segmented Manufacturing Requirement (if applicable)
    - If manufacturing is divided into multiple stages or segments, applicants must submit one of the following:
    - Option 1: QC flow chart for each individual stage.
    - Option 2: Joint audit documents that serve as supporting evidence of QC across all stages.
    a. Establish a sampling inspection mechanism and clear procedures to ensure each product batch meets consistent acceptance standards.
    b. Conduct stability testing to determine and validate product shelf life.
    c. Implement monitoring and audit systems to verify that quality management practices remain effective and continuously improved.
    Describe principles, structure, and procedures for handling emergencies. Provide customer complaint records, service management, and satisfaction survey analyses.
    Evaluate compliance with global quality and safety benchmarks.
  9. Safety & Hygiene (20%)
  10. a. Review usage instructions and precautionary statements.
    b. Confirm nutrition labeling compliance with Ministry of Health and Welfare standards for packaged foods.
    c. Provide batch numbers and expiration dates of submitted products.
    a. Review designated test items (e.g., microbes, heavy metals).
    b. Confirm compliance with regulatory testing requirements based on product attributes.
    c. Submit inspection reports issued within the past year or latest production batch, certified by accredited laboratories recognized by the Ministry of Health and Welfare.
    Provide records of violations within the past three years (if none, state "None").

Application Timeline

Online Application (Batch 1)
March – May
As announced in the annual call for entries
Online Application (Batch 2)
May – August
As announced in the annual call for entries
Document Submission (Batch 1)
May 31
Submit all required documents by the deadline
Document Submission (Batch 2)
August 31
Submit all required documents by the deadline
Review & Evaluation (Batch 1)
June – July
Includes administrative review, document review, presentation review, and the final review committee meeting.
Review & Evaluation (Batch 2)
September – October
Includes administrative review, document review, presentation review, and the final review committee meeting.
Announcement of Certification Results (Batch 1)
August
Certification results determined and certified institutions are required to sign the "SNQ Mark License Agreement," valid for one year.
Announcement of Certification Results (Batch 2)
December
Certification results determined and certified institutions are required to sign the "SNQ Mark License Agreement," valid for one year.
Renewal Application
Next July – September
Renewal application with required documents must be submitted within three months before certification expiry. Renewal applicants may also apply for the National Biotechnology & Medical Care Quality Award in the same application cycle.

Application Documents

Applies to|Pharmaceuticals, Traditional Chinese Medicines, Medical & Healthcare Devices, Clinical Support Services & Products, Smart Health Technology, Aging Health & Long-Term Care, Nutritional Health, Cosmetics, Epidemic Prevention Products, and Animal Care Services & Products categories

Application Steps

  1. 1
    Online Application

    All applications must be submitted online. Visit the SNQ official website (www.snq.org.tw) homepage and then click "Apply for Certification".

  2. 2
    Fill in the Form and Download Templates

    Log in to the "Application & Review Data Maintenance Portal" to complete the application form and download the required document templates.

  3. 3
    Pay the Fees and Upload Materials

    Pay the application fees and upload the required materials as specified. The application is considered complete only after the organizer confirms receipt.

Required Materials

  1. 1
    Application Consent Form

    Complete the online application form, print it, affix the institution's official and small seals, then scan and upload the signed copy as a PDF.

  2. 2
    Application Plan

    Prepare the plan per each category's template and upload as an unencrypted PDF. (Content must be complete and include supporting evidence.)

  3. 3
    Application Item Images

    (1) 3–5 photos (jpg or png, at least 1000 × 750px in 4:3 landscape, 300dpi or higher). Product entries must include a background-removed hero photo, centred and scaled so the product is fully visible with no part of it clipped by any edge; other close-up shots are exempt from this rule. Technology or service entries should show the theme, workflow, features, and team; nutritional health products additionally require close-ups of the packaging and labelling. (2) Applicant logo (jpg or png, 300dpi or higher).

  4. 4
    Product Samples (10 units)

    Provide 10 samples with complete inner and outer packaging identical to what is sold on the market; if multiple specifications exist, submit 10 of each. Deliver in person or by registered mail to "1F, No. 508, Sec. 7, Zhongxiao E. Rd., Nangang Dist., Taipei 115 - SNQ National Quality Mark Administrative Team". (Skip if no physical product exists; for oversized products, contact the coordinator to confirm the arrangement.)

Application Fees

Products
NT$ 100,000/ per item

Pharmaceuticals, Traditional Chinese Medicines, Medical & Healthcare Devices, Clinical Support Services & Products, Smart Health Technology, Aging Health & Long-Term Care, Nutritional Health, Cosmetics, Epidemic Prevention Products, and Animal Care Services & Products categories.

  • Applications that do not pass review (including ineligibility or failure at any stage, excluding revisions) will receive a refund within 30 days of the result announcement, after deducting NT$ 30,000 for administrative and review fees. Nutritional health products run in two application rounds; entries rejected in the first round may reapply for the second round after improvements, to encourage quality improvement.

  • Series product bundle applications are priced at NT$ 120,000 for two items, plus NT$ 20,000 for each additional item. Failed applications are refunded after deducting NT$ 30,000 for administrative and review fees.

Bundled Applications

Applicants may bundle multiple items submitted in the same year (same round) into a single application if the following conditions are met. A bundled application must submit one integrated plan covering the series (including each product's ingredient specification and related test reports).

Nutritional Health

The main ingredients and their amounts are identical, the nutritional components and their amounts are identical, and the health claims and efficacy are identical; the products must be produced by the same manufacturer using the same process and dosage form, differing only in flavour, taste, or colour.

Eligible for bundling
  • Organic rice crackers (Original)
  • Organic rice crackers (Apple)
  • Organic rice crackers (Carrot)
Not eligible for bundling
  • Vigor (Astragalus) essence of chicken
  • Wellbeing (Cynanchum otophyllum) essence of chicken
  • Divine (Four Divine Herbs) essence of chicken
Bundled applications submit a single plan; the fees are NT$ 120,000 for two items plus NT$ 20,000 for each additional item. Approved bundles share a single SNQ National Quality Mark certificate and authorization agreement; failed applications are refunded after deducting NT$ 30,000 for administrative and review fees. Annual renewal costs NT$ 20,000 per item. (Whether items qualify as a product series is determined at the organizer's discretion.)

Review Process

1
Administrative Review
Verify eligibility, category, and completeness of submitted materials.
2
Document Review
Reviewers assess applications based on defined criteria; comments provided for applicant response.
3
Presentation Review
Review committee presentation meeting and Q&A; scoring by criteria and weightings; results determine shortlist for site visits.
4
Final Review & Resolution
Committee finalizes certification results and determine winners of the National Biotechnology & Medical Care Quality Award

Review & Authorization

Result Notification & Mark Authorization

The organizer notifies applicants of the review results by formal written letter each August (first round) and December (second round) and publishes the selected list on the SNQ official website. Each selected unit must sign the "SNQ National Quality Mark Usage Authorization Agreement" with the organizer before the selected item may officially use the "SNQ National Quality Mark".

Sampling & Audits

  • After the announcement, the organizer randomly inspects the quality and mark usage of selected items through market channels; any violation of authority regulations or significant quality defect will result in revoked mark authorization, with full legal responsibility borne by the applicant.

  • The organizer conducts unscheduled on-site visits or paper reviews of manufacturing facilities; for factories located overseas, alternative measures beyond on-site visits are defined.

Renewal

Application Timeline

To ensure certified items maintain their quality, the annual renewal process begins each July. Applicants must submit renewal applications with all required documents at least three months prior to certification expiry.

Validity of Renewal

Approved renewals extend the authorization to use the SNQ Mark and allow continued participation in related promotional programs. The renewed authorization period is from January 1 to December 31 of the following year.

Eligibility for the National Biotechnology & Medical Care Quality Award

Renewal applicants may also apply for the current year's National Biotechnology & Medical Care Quality Award in accordance with that year's application procedures.

Failure to Renew

Applicants who fail to submit a renewal application within the specified timeframe will lose authorization to use the SNQ Mark upon expiry and will not be eligible for further renewal.

Application Fees

The renewal administrative and review fees are NT$ 20,000. Applicants who also enter the current year's National Biotechnology & Medical Care Quality Award pay NT$ 30,000. (No additional refund is given if the renewal or award bid is unsuccessful.)