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.
Interfarmax has valid pharmaceutical licences for drugs and controlled substances. Pharmaceutical license was permanently issued on the 14th of December, 2006. Pharmaceutical license for controlled drugs was permanently issued on the 25th of April, 2007. Interfarmax has GDP and ISO 9001 accreditations and annual inspections by Bureau Veritas since 2012. ISO 9001 certificate was first issued on the 10th of July, 2012. GDP certificate was issued on the 28th of May, 2019.
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.