Manufacturing

Polpharma Santo has a modern high-tech production of medicines of various forms and dosages that are the most in demand by the healthcare system. The company's priority is the efficacy and safety of medicines, which is ensured by the strict adherence to national and international GMP quality standards by all employees and processes. This is what makes Polpharma Santo one of the most sought after and reliable partners.

17га
Plant area
170+
Near generics
1200+
Employees all over Kazakhstan

Our technologies

One of the best research laboratories in the country.
Our own research and test center as well as laboratories of the quality control department allow us to conduct researches, use the latest technologies, guarantee the quality and efficacy of our medicines, and also develop new products.
The production facilities are equipped with modern equipment by leading world manufacturers. Employees demonstrate professional competence and expertise as well as go ahead with their continuous development.
The quality of medicines is ensured at all stages of the product life cycle: from drug development to the sale stage.

Pharmacovigilance

Please report data on side effects of medicines and medical inquiries to the following address
+7 (725) 261-01-50
+7 (701) 883-02-30 +7 (702) 208-62-92 +7 (701) 401-04-94
For information on side effects (Download form) :

For information on side effects (Download form) :

Consent to the collection and processing of personal data
(Download file)

Manufacture

GMP Certificates
February 02, 2024
EurAsEU GMP EurAsEU GMP GMP certificate for the production of oral solids

Valid until February 01, 2027
May 10, 2023
GMP UZ GMP Certificate for the Production of: • Parenteral Forms (Injections), • Oral Liquid Forms, • Oral Solid Forms

Valid until September 12, 2027
March 20,2025 EU GMP
GMP ЕU certificate for production site of department No. 3 for solid oral drugs

Valid until May 14, 2028
April 22, 2025 EurAsEU GMP
EurAsEU GMP certificate for the production of parenteral and oral liquids

Valid until April 21, 2028
April 23, 2025 EurAsEU
GMP EurAsEU GMP certificate of aseptic filling of antibiotic powders of Cephalosporins

Valid until April 24, 2028
January 31, 2024 EurAsEU GMP
EurAsEU GMP certificate for the production of parenteral and oral liquids

Valid until January 30, 2027
15.05.2025 GMP EU
Certificate of GMP compliance for a manufacturer

Valid for 3 years from inspection date
17.04.2026 cGDP
Certificate of Good Distribution Practice compliance

Valid until: 17.02.2029
30.01.2026 GMP EAEU
Certificate of GMP compliance of pharmaceutical manufacturing with EAEU GMP Rules

Valid untill: 29.01.2029