19A-5 Zviozdnaya str.,
223028 Minsk region, vBelarus
Clinical Trials Project Management
Tel./Fax +375 17 543 00 17
Interfarmax is constantly developing and improving policies in on the quality of services. All personnel engaged in clinical trials is regularly trained in accordance with the GDP / GMP requirements.The system of standard operating procedures (SOP) describes in details our logistics services. Our all SOPs meet the all requirements of GDP (GMP), ISO 9001:2008, international standards and national legislation.
For the time being we have acquired a reputation for being a professional and reliable partner. We have established a high-quality up-to-date specialized depot for clinical trials that meets the requirements of world standards. Our customers from different countries held numerous audits. During the audits a high level of our quality management system was marked. We don't stop and keep on developing. but the company is continuing to improve it.
Certification of our compliance with the requirements of ISO 9001:2008 by «Bureau Veritas» is scheduled on 2012. Certification to meet the requirements of GMP/GDP is scheduled for the end of 2012 – start of 2013 years.
Interfarmax was ISO 9001:2008 certified by Bureau Veritas in 2012. Certification to meet the requirements of ISO 9001:2015 is scheduled for the 1st guater of 2018.
Interfarmax has valid pharmaceutical licences for drugs and controlled substances.