Regulatory compliance is one of the most critical aspects of pharmaceutical exports. Importers in Russia and CIS countries require proper documentation to ensure product safety, quality, and legal compliance.
Key documents typically include Drug Master Files (DMF), Certificates of Analysis (COA), WHO-GMP certificates, and product specifications. These documents confirm that the product is manufactured in compliance with international quality standards and is suitable for regulatory submission and import approval.
At GANGA-VOLGA, regulatory documentation is treated as a core part of our sourcing process. We work closely with manufacturers to ensure that all required documents are available, verified, and aligned with the importer’s regulatory needs. This documentation-driven approach helps reduce delays, minimize compliance risks, and build long-term trust with our clients.