GMP

GMP INTRODUCTION INTO CHIMPHARM JSC

20 February 2018 – CERTIFICATE of compliance with the requirements of the good pharmaceutical practices in the area of circulation of medicines “GOOD MANUFACTURING PRACTICE STANDARD” to the production site for the manufacture of solid oral medicines.

20 February 2018 – CERTIFICATE of compliance with the requirements of the good pharmaceutical practices in the area of circulation of the medicines “GOOD MANUFACTURING PRACTICE STANDARD” to the production site for the manufacture of injection solutions and infusions.

2 March 2018 – CERTIFICATE of compliance with the requirements of the good pharmaceutical practices in the area of circulation of the medicines “GOOD DISTRIBUTION PRACTICE” to the pharmaceutical warehouse.

February 22, 2019 – CERTIFICATE of compliance with Medicines Circulation GPP «PRODUCTION LINE OF ORAL LIQUID MEDICINAL PRODUCTS» for GMP compliance.

July 23, 2019 – CERTIFICATE of compliance with the requirements of good pharmaceutical practices in the area of circulation of medicinal products for compliance with the standard of GOOD MANUFACTURING PRACTICES for the production site aseptically filling antibiotic powders that are classified in the cephalosporin group (Department No. 2 for aseptic filling of antibiotic powders).

February 28, 2020 – CERTIFICATE of compliance with the requirements of good pharmaceutical practices in the area of circulation of medicinal products for compliance with the standard of GOOD MANUFACTURING PRACTICES for the production site aseptically filling antibiotic powders of the beta-lactam group (carbapenems), aminoglycosides and polypeptide antibiotics (Department No. 2 for aseptic filling of antibiotic powders).


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