Good Manufacturing Practice (GMP) documents are required for the effective distribution of medicines. GMP documentation is mandatory for a proper application submission in the Eurasian Economic Union region.

We offer the subsequent services for GMP inspection and application submission in the Eurasian Economic Union:

  • Consultations and support on Good Manufacturing Practice inspections in the EAEU
  • Preparations and submissions of the applications
  • Translation of documents
  • Provision of the translator/accompanying person, if needed
  • Analysis and support with CAPA responses

For any inquiry regarding our services, please contact Biomapas Business Development team.

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