FAQ
Yes, we carry out contract manufacturing and private label projects for our clients developing their own brands. We offer comprehensive support including recipe development, packaging selection, documentation preparation, and production of the finished product tailored to the individual needs of the brand.
We can provide a comprehensive manufacturing service, taking responsibility for sourcing raw materials and packaging, work with materials supplied by the client, or use a hybrid model. The exact division of responsibilities is agreed individually for each project.
Yes, all finished products are manufactured in accordance with the applicable requirements and quality standards in force on the European Union market. The production process and documentation take into account current regulations regarding the safety, quality, and labeling of dietary supplements and functional beverages.
Yes, we comprehensively support clients at every stage of product creation — from concept and selection of active ingredients, through recipe development, to preparing the product for implementation and mass production. We also advise on product functionality, form of administration, and selection of raw materials meeting market expectations.
Yes, we provide support in preparing product documentation and verifying labeling in accordance with current EU market requirements. We help our clients, among other things, in developing specifications, preparing label information, and correctly designating active ingredients.
FAQ
Each production batch is monitored and documented at all stages of the process — from raw material acceptance to the finished product. The quality systems in place at our production facility ensure full traceability of components and control over all stages of the production process.
The MOQ depends primarily on the product type, dosage form, formulation, availability of raw materials and packaging, and the technological requirements of the production line. Equipment setup, changeover and sanitation costs are also taken into account. The minimum batch size is determined individually after reviewing the project.
The rules governing confidentiality and the use of the documentation provided are set out in the agreement. Before detailed work begins, a non-disclosure agreement (NDA) may be signed to protect the formulation, commercial information and all other project-related data.
Each production batch is monitored and documented at all stages of the process — from raw material acceptance to the finished product. The quality systems in place at our production facility ensure full traceability of components and control over all stages of the production process.
The timeline depends on the project’s complexity, the availability of raw materials and packaging, the number of production trials required, the scope of testing and the order volume. Once the project requirements have been reviewed, we prepare an individual implementation schedule.
