Most pharmaceutical manufacturers who approach FarmBioVet with requests for designing the production of APIs from plant raw materials, as a rule, only know the final product, but do not have the technology for its production. In the best case, our Customers have only laboratory regulations that need to be verified, and then scaled and optimized.   

In such a situation, it makes sense to start the project implementation with the development of a Feasibility Study (project feasibility study). Earlier, in Soviet times, a combination was also used: Feasibility study (FS). The scientific and technological team of FAVEA-Center, first of all, focuses on determining the technical and technological parameters of the future project.

 

Before starting the development of the Feasibility Study, the FarmBioVet team is required to complete the following preparatory work:

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1.   Define and record the objectives of the project, describe the types of products, make a list of the standards and regulations used (national and international).

2.   Conduct an analysis of the planned production program, compare with similar or similar projects previously implemented by FAVEA specialists. At this stage, our specialists study the available initial data for design, the main characteristics of the product, determine the toxicological categories of active substances according to OEV / OHC, the features of the processing technology of each drug, the number of isolation stages.

3.   Conduct an analysis of the input plant material that will be used for the production of API.

4.    Perform a literary and patent analysis of possible technologies for the production of products.