LDV - group - progressive, dynamic company was founded in April 2011 and has been successfully operating in the pharmaceutical market for over 8 years.
Taking into account the requirements of the modern pharmaceutical market, our company provides systematic educational and informational support for the modern pharmaceutical world. We are in constant cooperation with the leading research organizations, companies, manufacturers and medical institutions in the Russian Federation, the CIS countries, Europe to inform about the development of innovative medicines that open up new directions in medicine, as well as to perform a detailed analysis of safety, efficiency, and new properties of drugs already in circulation.
We offer our Customers to voluntary audit of manufacturers of pharmaceutical products and manufacturing sites, and condition of the Customer's production facilities in accordance with GMP EU standards (European Union Good Manufacturing Practice) on compliance with the Good Manufacturing Practice, approved by Order of the Russian Ministry of Industry and Trade No. 916 "On Approval of Rules of Good Manufacturing Practice” of 14 June 2013, registered in the Russian Ministry of Justice on 10 September 2013, No. 29938.
Our Company’s policy is aimed at the possibility of providing regulatory support to developers, manufacturers of medicines, contract research organizations, companies providing services for the registration of drugs, bioanalytical laboratories to simplify the development and increase the availability of high-quality, effective and sufficiently safe medicines to protect interests patients.