1.Analytical-normative documentation for medicines; 2.Application for finish form of medicines; 3.Stability report till full term of storage of the medicines; 4.Technological schema of production of the medicines; 5.The list of organic solvents used on all stages of manufacturing of medicines production and intermediates (ingredients) production; 6.The Certificate of Analyses and short characteristics for the substance; 7.Pharmacological and toxicological documentation; 8.Human health hazards of the substance; 9. Human health hazards of the intermediates, ingredients; 10.Ecological information; 11.Firefighting properties and measures.
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