Preparation of pharmaceutical production sites engaged in or planning to produce medicines of any form, to obtain primary, as well as to expand the existing license, GMP certification of the EAEU.
Consultations on the development and production of new dosage forms and substances, development of the pharmaceutical quality system, localization of production and technical development of production sites.
Search, analysis and evaluation of the quality system, production conditions and quality control of manufacturers of pharmaceutical substances and auxiliary materials for compliance with GMP rules.
Organization of preclinical and clinical trials for registration of medicines, consulting on compliance of testing laboratories and centers with GLP requirements.
Registration, promotion and distribution of medicines
Promotion of new pharmaceutical products to the markets of Russia and the EAEU, including the organization of marketing activities, search for distributors and registration of trade organizations.
Solving a set of tasks for the search, audit and establishment of the release of medicines at third-party pharmaceutical production sites in Russia and abroad.