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[/tab] [tab title=”2012″]
In October 2012, a warehouse of organic chemical agents with a total area of 1,400 square meters was launched.[/tab][tab title=”2013″]
In 2013 a microbiological division became part of the quality control laboratory.
New Class D classified clean rooms were commissioned [/tab] [tab title=”2014″]
In May 2014 a new warehouse for alcohols, precursors and flammable liquids with a total area of 425 cubic meters was built.[/tab] [tab title=”2015″]
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[/tab] [/tabs]