Registration of food supplements

To introduce a food supplement of foreign manufacture into the Ukrainian market it is necessary to receive an international health certificate for this type of product from the country of origin of the product, and in case of necessity to carry out scientific research examination and assessment of documents on the food supplement for conformity to the current requirements of the Ukrainian laws.

A domestic manufacturer shall have registered regulatory documents for production and carry out assessment of products for conformity of the current requirements of the Ukrainian laws.

Moreover, any market operator, activity of which is related to food supplements, on all stages of production and circulation shall provide conformity of food supplements to the Ukrainian laws of food products.

What is the process of introduction of food supplements into circulation in Ukraine?

Examination of food supplements can be carried out only at specialised accredited organisations – laboratories, institutes, and scientific research centres.

Types and terms of works depend directly on the composition, recommendations for use, age restrictions, and any other characteristics of a food supplement.

The process of introduction into circulation lasts about 1 month and includes such steps:

detailed analysis of technical documents and accompanying documents

preparation and submission of an application together with draft marking, samples for laboratory testing, and accompanying documents for the competent authority

support of examination on all stages, particularly communication with experts

development of packing materials according to the current laws

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preliminary consultation and development of a regulatory strategy

professional analysis of technical documents

translation of required documents

agreement of accompanying documents, particularly an international certificate

completeness and execution of technical documents for submission to the competent authority

development of draft marking of packing and a product instruction

support of import of sample products for laboratory testing

submission of an application, technical documents and samples for laboratory testing

complex follow-up support of the procedure of examination, particularly provision of additional materials and communication with experts

control over observance of terms on all stages of examination

development and implementation of packing

Result-oriented high-quality service!

MAXIMA Health Research with long-term experience in registration and post-registration support of different kinds and types of products has profound knowledge of requirements of the current laws and offers you to carry out any required regulatory procedures qualitatively and quickly, and most importantly according to the current laws and strategy of the company.

Our company successfully provides services for regulatory activity to pharmaceutical and FMCG companies, so we are ready to answer any of your questions.

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Regulatory Intelligence in Life Sciences

Contact information

The office of MAXIMA Health Research is located in the office center of Delta Medical, at the address:
st. Chornovola, 43, Vyshneve, Kyiv region, 08132, Ukraine

tel.: +38 (044) 593-38-86
tel.: +38 (044) 593-33-55
fax: (044) 593-33-54

info@maxima-health.com

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