About us

Research laboratory

research-laboratory
Production Sites

production-sites
lab_6

microbiological
Warehouses

warehouses
Clean premises

clean-rooms
lab_3

About us

The production base of PHARMHIM LTD. was formed in 2002. During several years, the company was releasing a single product - mebhydrolin (substance for the manufacture of diazolin) - and is the only CIS manufacturer of this substance that has antihistamine properties.
In 2008, we initiated the production of unpurified dioxidine - the main raw material for further production of pharmaceutical substance, which increased the volume of production and sales.
Starting from 2009 the company is constantly expanding the range of its own production, namely building new manufacturing sites and developing the production of new products.
In 2010 new specialized facilities complying with licensing conditions and other requirements for the excellent conduct of the process and quality control were constructed.
In 2011 a laboratory of quality control department was launched. In 2011, the company has been certified for compliance with international State Standard of ISO 9001: 2009 New Class D classified clean rooms were commissioned
In October 2012, a warehouse of organic chemical agents with a total area of 1,400 square meters was launched.
In 2013 a microbiological division became part of the quality control laboratory. New Class D classified clean rooms were commissioned
In May 2014 a new warehouse for alcohols, precursors and flammable liquids with a total area of 425 cubic meters was built.
The laboratory of quality control department at PHARMHIM LTD. has been certified for the right to perform quality and safety control of medicines. PHARMHIM LTD. has the Certificate of good manufacturing practice compliance (CERTIFICATE OF GMP COMPLIANCE) New Class D classified clean rooms were commissioned
The laboratory of the quality control department of PHARMHIM LTD has been certified for the right to conduct quality control and medicine safety assurance.
PHARMHIM LTD received the Certificate of Compliance with the requirements of good manufacturing practice (CERTIFICATE OF GMP COMPLIANCE) The production of medicines ALBROFEN (solution in bulk) and PHENIBUT (API) was mastered.
The registration certificate of the Ministry of Health of the Republic of Belarus for the company’s products was received.
New classified rooms of D cleanliness class were commissioned.
The work on expanding the product portfolio was intensified. The company began to produce 3 new medications: Glycine, DL-camphorsulfonic acid , Menthol solution menthyl ester of isovaleric acid.
The production of Pyridoxal-5-phosphate and Novocaine base was mastered.
The registration certificate of the Ministry of Health of the Republic of Belarus for 2 active pharmaceutical ingredients was received.

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