Europe (PRWEB) January 25, 2016
Biomapas, a contract research organization strengthened its Eastern European presence by opening a new office in Ukraine. “Biomapas continues to expand its Eastern European footprint to meet the needs of our clients. We are playing a bridging role between East and West, supporting Pharma and Biotechs in clinical trials, regulatory affairs and pharmacovigilance services” said Managing Director, Audrius Sveikata.
Formed in 2001 from the local Lithuanian CRO, Biomapas expanded into a leading Eastern European CRO, providing services including clinical development, site selection, monitoring, regulatory affairs, pharmacovigilance and full clinical trial management, with a particular focus strength in oncology, neurology, and cardiovascular diseases.
Biomapas has offices in Switzerland, Lithuania, Russia, Belarus and Georgia. The CRO also has reach in the whole Europe, in a partnership with an Association of international CROs (AICROS).
The pledge to open a new office in Ukraine demonstrates the ongoing commitment to strengthen the regional presence of Biomapas. Local presence will guarantee process optimization and smooth project implementation. With a great focus on European quality standards, we ensure a more attentive and individual approach to every partner and project in Eastern Europe.
In 2014, Ukraine came under the spotlight. Yet, this country proves its capacity to meet the tight deadlines, and enables high recruitment rates. With a population of 50 million, and international increasing clinical trials Ukraine is back on the map for clinical trials.
With headquarters in Lithuania, Biomapas CRO is a team of experts, specializing in Phase I-IV clinical trial monitoring and project management, Regulatory Affairs, Marketing Authorization Approvals, and Pharmacovigilance services. We are focused on the delivery of quality services to the pharmaceutical, biotechnology and medical device industries.
Biomapas is certified to be in compliance with ISO 9001 standards, providing a variety of services: Clinical Trial Management and Monitoring, Project Management, Site Management, Post-Marketing Studies, Clinical Safety, QA, Data Management, Regulatory Affairs, Pre-submission Assessment and Consulting, Marketing Authorization Applications and submissions, Package Leaflet Readability Testing, Medical Writing, Electronic Submissions, Pharmacovigilance, GCP Training, Full-service CRO.
For more information, please contact:
Audrius Sveikata, M.D., Ph.D., Managing Director Biomapas +370 3736 6307 info(at)biomapas(dot)eu
To learn more about Biomapas, please visit http://www.biomapas.eu