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TO REGISTER AND SELL MEDICINES in Kazakhstan or other country you are required to have:
- – medicines’ master files;
- – periodic safety reports;
- – main information on safety;
- – specifications at release and shelf life;
- – summary of a product characteristics;
- – analytical procedures;
- – quality control documentation;
- – clinical trials protocols;
- – individual record sheets;
- – clinical expert reports;
- – medication guides;
- – equipment specifications
- and other documents.
You can learn more about the rates below. The rates are indicated for 1800 characters with spaces (which is about 1 typed page).
We offer the best quality at the most competitive prices!