The full path of the implementation of a dietary supplement - from the idea to the finished product

How is the recipe development phase going?

The introduction of a new preparation on the market requires going through a multi-step process, covering both laboratory work and legislative procedures. Each phase, from the selection of raw materials to the final packaging, must be carried out in accordance with strict quality standards. We invite you to read the detailed analysis of the implementation cycle.

The process begins in the research and development (R&D) department, where technologists verify the active ingredients for their interactions and market availability. The key task is to determine the doses of active substanceswhich must be within the safe limits provided for food. Only after approval of the theoretical formula, technological tests are carried out to verify the physical form of the preparation and its behavior in the molding process. At this point, it is also worth determining the target audience, which determines the choice of the form of administration, e.g. softgel capsules that are easy to swallow.

When does proper production and legalization take place?

In parallel with the work on the composition, it is necessary to prepare the documentation necessary to notify the competent sanitary authorities of the placing of the product on the market. Properly planned contract production of dietary supplements It also includes the purchase of certified raw materials and the implementation of the manufacturing process in accordance with the GMP standard. This stage requires close monitoring of environmental parameters, such as humidity and temperature, to ensure the physicochemical stability of the product.

Why does quality control end the implementation process?

Finished forms, such as capsules or tablets, go to packaging, where they are packaged in blisters or jars and labeled in accordance with the requirements of food law. Before the batch is released to the warehouse, microbiological analyzes are carried out and tests for impurities confirming the purity of the product. Only obtaining positive results from an accredited laboratory allows the safe distribution of goods to the final recipients.

The most important information — the path of implementation of dietary supplements

The implementation cycle begins with conceptual work in the laboratory, where the recipe is established, the interactions of the ingredients are studied and technological trials are carried out. The next step is the formal legalization of the product and the implementation of production in a sanitary regime, taking into account the strict control of the parameters of the environment. The whole thing closes the stage of packaging combined with rigorous quality tests, which condition the final admission of each batch to market.

FAQ

What does the R&D department do at the beginning of cooperation?

Specialists verify the composition for safety, determine the dosages of the substance and check the potential interactions between the components. At this stage, trial batches are also created to evaluate the physical characteristics of the product.

What conditions must prevail during manufacturing?

The process takes place in a controlled environment, where the temperature and humidity of the air are constantly monitored. This is necessary to preserve the stability of raw materials and meet the standards of Good Manufacturing Practice.

What determines the release of a product for sale?

A prerequisite is a positive result of the final analyzes, which include microbiological and physicochemical studies. Only confirmation of purity and compliance with specifications makes it possible to hand over the goods for distribution.

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