Production

“NOVOPHARMA PLUS” JV LLC has 2 workshops operating independently from each other on the production of ampoule filling injection solutions and dry powder antibiotics. Workshops are equipped with up to date and highly reliable equipment meeting international quality standards. All production units are well organized with clean rooms of the highest purity “A” and “B” grades

The plant is equipped with air conditioning and clean water supply.

The whole production process is controlled by Quality Assurance Department.

Ministry of Health of the Republic of Uzbekistan and “UZFARMSANOAT” State Joint Stock Concern accepted “NOVOPHARMA PLUS” JV LLC as a model factory for the pharmaceutical industry.

Production of ampoule filling injection solutions.

Up to date production lines at the plant are capable of producing medicines in 1 ml, 2 ml, 5 ml, 10 ml ampoules. Ampoule production is based on the method of syringe filling, which results the highest possible level of purity and dosage accuracy. Water for injection solutions goes through a multistage process of filtration and deionization. The company has introduced advanced technology of water treatment - reverse osmosis. This cleaning method protects virtually any impurities even from low-molecular inorganic compounds, atoms and ions whose size makes 1/1000 fraction of a micron.

Production of dry powder medicines

The production line of dry powder antibiotics is set up under ISO international quality standards.

The dry powder equipment in the workshop allows filling pharmaceutical powder substances into 7 ml, 10 ml, 15 ml, and 20 ml flacons. Ultrasonic washing machine and a microprocessor of metering filling provide absolute sterility and the maximum accuracy of a dosage of produced antibiotics.

Quality Control

Pharmaceutical production is a complex technological process and the quality, efficacy and safety of medicines depends on careful work out and production in various stages. Therefore, the company organized Quality Assurance Department (QAD), Quality Control Department (QCD) and Testing Laboratory.

Quality Assurance Department implements and supports quality assurance system in the production of pharmaceutical products. The department carries out the introduction of appropriate documentation systems according to the GMP (Directions 2003/94/EC) and ISO 9001:2008 requirements that maintains quality and control in all production units.

Quality Control Department constantly monitors the requirements of national and international quality standards and takes corrective actions from possible deviations from the established requirements through its specialists in the production units. Quality Control Department also organizes and carries out activities aimed at quality assurance. 

Testing Laboratory of “NOVOPHARMA PLUS” JV LLC is equipped with up to date high precision European equipment produced by SIEMENS, BOSCH, GRUNDFOS Companies for chemical, physical and microbiological analysis. The laboratory carries out multi-stage control system of condition of raw and auxiliary materials, manufacturing process and finished products. Also the laboratory carries out regular monitoring of air, industrial clothing and technological surfaces in production units. In June, 2010 the laboratory was accredited by “UZSTANDARD” Agency (Ref.: UZ.AMT.07.MAI.771) for technical competence under O `z DSt ISO / IEC 17025:2007 standard, which enables the company to control and analyze, microbiological research not only for “NOVOPHARMA PLUS” JV LLC, but also for other pharmaceutical companies. 
 
The departments obtained of ISO and GMP certificates for compliance with international quality standards in 2007-2008, and further re-certification under ISO 9001:2008 with the introduction of company information in an international IQNet database (Ref.: 378418 QM08) in 2010.