EU Compliance Platform for Botanical Medicines

Supporting the EU Market Entry of Botanical Medicines, Traditional Chinese Medicines, and Natural Health Products

As global demand for natural health products, botanical medicines, and Traditional Chinese Medicines (TCM) continues to grow, more companies are seeking opportunities to enter the European market. However, the EU regulatory framework for botanical and herbal products is highly complex, involving product classification, ingredient compliance, historical use requirements, quality standards, CMC documentation, clinical and non-clinical evaluation, as well as GMP compliance.


CCIC Europe Food Test B.V. provides comprehensive regulatory and technical support to help companies successfully navigate the EU market. Our services include regulatory assessment, registration strategy delopment, technical consulting, compliance evaluation, and market access support for botanical medicines, TCM products, herbal health products, and other natural products.


With extensive experience in EU regulations and industry requirements, CCIC Europe Food Test B.V. helps clients improve compliance efficiency, reduce registration risks, and accelerate international market entry.


Who We Support

We support companies, research institutions, and industry organizations involved in:


  • Botanical medicines
  • Traditional Chinese Medicines (TCM)
  • Herbal and natural health products
  • Food supplements and functional products
  • TCM extracts, granules, and botanical raw materials
  • Innovative botanical product development
  • Internationalization and EU market entry projects for TCM and natural products


Our services are designed for businesses seeking regulatory compliance, technical support, product registration, and sustainable expansion into the European market.

Core Services​

I. Feasibility Assessment for EU Health Product Notification


This service supports companies planning to introduce health products, food supplements, and natural products into the European market.

Based on the product formulation, dosage form, intended use, and target market, CCIC Europe Food Test B.V. provides a preliminary regulatory assessment to evaluate the feasibility of positioning the product within the EU regulatory framework and identifies suitable market entry pathways.


Service Includes:

  • Preliminary assessment of ingredient and formulation compliance
  • Evaluation of dosage form and intended use
  • Feasibility assessment for EU health product notification
  • Identification of potential regulatory risks and compliance challenges
  • Regulatory recommendations and market entry guidance
  • Professional consultation and project communication support

II. EU Traditional Herbal Medicinal Product (THMP) Feasibility Assessment


This service is designed for companies considering the Traditional Herbal Medicinal Product (THMP) registration pathway in the European Union, particularly for products supported by traditional use history or established herbal applications.

CCIC Europe Food Test B.V. conducts a comprehensive feasibility assessment covering formulation suitability, historical use evidence, regulatory pathway analysis, dossier readiness, and key compliance considerations for EU traditional herbal medicinal product registration.


Service Includes:

  • Assessment of product formulation and active ingredients
  • Preliminary evaluation of historical use evidence and supporting documentation
  • Regulatory pathway analysis for THMP registration
  • Dossier readiness and gap assessment
  • Identification of regulatory risks and development considerations
  • Strategic recommendations for registration and market entry

III. EU Scientific Advice for Innovative TCM & Botanical Products



This service supports innovative Traditional Chinese Medicine (TCM) and botanical medicine projects seeking regulatory guidance on product development and EU registration strategy.

CCIC Europe Food Test B.V. assists clients in preparing and submitting scientific advice applications to European regulatory authorities, including the Dutch Medicines Evaluation Board (CBG-MEB), and provides professional support throughout the consultation process.


Service Includes:

  • Preparation and structuring of scientific advice questions
  • Review of product development background and technical documentation
  • Support for scientific advice application submission
  • Regulatory consultation on registration strategy, clinical and non-clinical development, and CMC-related topics
  • Interpretation of regulatory feedback and strategic next-step recommendations
  • Ongoing technical and regulatory communication support throughout the project process

Contact Us​

If you are evaluating EU market opportunities for botanical medicines, Traditional Chinese Medicines, herbal health products, or related natural products, we welcome you to contact us for further discussion and preliminary project assessment.