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.