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.
Work Stages
Production Site Search
Search for a production site according to the requirements and wishes of the customer, advising the customer on the advantages and disadvantages of the proposed options
Production Site Audit
Assessment of the quality system, production conditions and quality control of the production site for compliance with the EAEU GMP Rules
Technology Transfer
High-quality and careful transfer and adaptation of production technologies, knowledge and research results to new production locations, taking into account established standards and requirements
Changes to the Registration Documentation and Launching Production
Making changes to the license documentation of the production site and registration dossiers of medicines, launching and setting up the production process
Contact Us
Phone/Whatsapp/Telegram +7 996 716 83 66
E-mail info@mpmadviser.com
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