What we do
Biomapas provides Clinical Trials, Regulatory Affairs, Medical Writing, and Pharmacovigilance services.
We are a team of international professionals supporting Pharmaceutical, Medical Devices and Biotech Companies for more than 15 years.
To combine the strength of our expertise, experience, and high quality deliverables to advance clinical development, market access and post-approval support to the Pharmaceutical and Medical Device industries improving health of patients.
Biomapas is a full-service clinical research organization (CRO) providing Phase I-IV Clinical Research, Regulatory Affairs, Medical Writing and Pharmacovigilance services for the pharmaceutical, biotech and medical device industries. Our expertise spans through various therapeutic areas, such as oncology, CNS disorders, cardiovascular diseases, rheumatology, pulmonology, cardiology, dermatology, etc.
Vidmantas Fokas, MD, PhD
Vidmantas Fokas has co-founded CRO Biomapas in 2001. Before becoming Chief of the Board, Vidmantas has been leading Biomapas as a Managing Director for over 10 years. His expertise includes clinical development strategies in EU and CIS, as well as extensive knowledge in business management. As a Chief of the Board, Vidmantas oversees business development, financial and commercial operations in order to provide his input in company's growth. With substantial knowledge in pharmaceutical industry, Eastern European and CIS markets, Vidmantas has highly contributed to the expansion of Biomapas into the CIS region. Being an urologist by training, Vidmantas also holds a Doctor degree of Medicine.
Prof. Audrius Sveikata, MD, PhD
Audrius Sveikata has over 20 years of experience in clinical research and regulatory affairs, holding executive positions within competent authorities, academia, pharmaceutical industry and professional associations. His expertise includes design and implementation of clinical development plans and regulatory strategies in EU. Prior to co-founding CRO Biomapas, Audrius was Head of Clinical Assessors unit at State Medicines Control Agency of Lithuania. As a professor of pharmacology at Lithuanian University of Health Sciences, Audrius was involved in teaching and science with specialization in neuro-psychopharmacology. He is active as a lecturer in various life science conferences, a co-author of over 50 scientific publications.
Gytis Bendorius, MD, MM
Gytis Bendorius has joined CRO Biomapas as a Member of the Board in 2014. Gytis has over 20 years of experience in pharmaceutical industry, business management and strategic planing. Prior to joining Biomapas Board, Gytis has been holding lead positions and serving as a Commerce and Managing Director at Tamro Lithuania and Tamro Baltics (PHOENIX group company), General Manager at Neptuno Vandenys JSC, Chairman of the Board of Lithuanian Pharmaceutical Wholesalers Association. At present, Gytis is a Managing Director at MediFocus JSC. Gytis is a medical doctor by training and also holds a Master degree of Management obtained at ISM University of Management and Economics.
Chief Executive Officer
Prof. Audrius Sveikata, MD, PhDProf. Audrius Sveikata has over 20 years of experience in clinical research and regulatory affairs, holding executive positions within competent authorities, academia, pharmaceutical industry and professional associations. His expertise includes design and implementation of clinical development plans and regulatory strategies in EU. Prior to co-founding CRO Biomapas, Audrius was Head of Clinical Assessors unit at State Medicines Control Agency of Lithuania. As a professor of pharmacology at Lithuanian University of Health Sciences, Audrius was involved in teaching and science with specialization in neuro-psychopharmacology. He is active as a lecturer in various life science conferences, a co-author of over 50 scientific publications.
Chief Financial Officer
Edgaras Kabecius, MEconEdgaras Kabecius has over 10 years of experience in corporate finance. His expertise includes business development processes, implementation of various IT systems into company's activities, valuation of investment projects and analysis for manufacturing, retail and real estate industries. At Biomapas Edgaras is responsible for ensuring efficiency of the the companies finance function and implementation of Biomapas strategy. Edgaras holds a Bachelor degree in Econometrics, as well as Master degree in Economics.
Director Quality Assurance
Egidija Pauriene, MDEgidija Pauriene, MD manages and ensures the quality systems. She helps guide the integration of the corporate strategies of Biomapas Group related to GxP Quality Assurance, regulatory compliance, including Good Pharmacovigilance Practice and ISO 9001:2015 standards. She has conducted and supervised GxP audits, as well as audits to CROs, and Suppliers. Edigija is a member of Research Quality Assurance, Investigator GCP trainer, Member of Society of Infectologist.
Diana Marija Lopsaitiene
Director Human Resources
Diana Marija Lopsaitiene, BA, BBM, MOPDiana Marija Lopsaitiene has joined CRO Biomapas as a Director Human Resources in 2016. Diana has over 12 years of experience in Human Resource Management. Prior to joining Biomapas team, Diana held HR positions with increasing responsibility in leading international and local companies - HR Manager at Swedbank, HR Projects Manager at Topo Group, Head of HR at Kelprojektas and HR Projects Specialist at Mondelez International (prior Kraft Foods). Diana’s expertise includes HR strategy, performance management, employee motivation, compensation and benefits, recruitment and talent search, employee development and engagement, career planning, management change, labor law. Diana holds Bachelor degrees in Psychology and Business Management, as well as Master degree in Organizational Psychology.
Associate Director Business Development
Egle Pavyde, MPharm, PhD candidateBeing a Pharmacist by training, Egle Pavyde has continued her studies as a PhD candidate in stem cell research. She is a co-author of 5 scientific publications. After working for 7 years in scientific research and 3 years in academia, Egle took a great opportunity to join CRO Biomapas as a lead in Regulatory Affairs Department. Managing personnel and a number of different complexity projects, she has gained a valuable experience from the operational side. At the same time Egle was responsible for business development of Regulatory Affairs Department. Anticipating to be more involved in company's expansion, strategic planning and decision making, Egle has been transferred to Business Development Department, becoming responsible for BD activities of all 3 operational departments of Biomapas.
Director Clinical Operations
Indre Dryziene, MBIIndre Dryziene has a strong expertise in Clinical Trials, with over 12 years of experience in the CRO setting and management of clinical research activities across the European and CIS markets. As an experienced business professional, Indre was involved in the business development and strategic management of Biomapas. Over the last 10 years she held various positions, such as a Managing Director and Member of the Board. Indre holds a Master Degree in Business Information Technologies. On the top of it she is certified in Strategic Management and Marketing Strategy from ISM University of Management and Economics.
Nidas Jurjonas, MDNidas Jurjonas has almost 20 years of experience in hospital and industry settings in Eastern Europe, Scandinavia and the United Kingdom. His expertise includes Disease Area Leadership for Europe in one of the biggest pharma companies. Prior to joining Biomapas Nidas had various leading roles in Medical Publishing, Medical Affairs, R&D, Medical Excellence, Compliance and Quality. Having a background of Internal Diseases physician, his key areas of focus were Haematology and Oncology. On the top of the MD background, Nidas holds a Master degree in Economics with the particular professional interests for Health Economics and Pharmacoeconomic modelling. He is a co-author of 7 scientific publications.
Director Regulatory Affairs
Laura Monkiene, MPharm, MBAMrs Monkiene has more than 7 years of experience in the CRO environment in the area of Regulatory affairs. Laura provides interpretation, guidance, and advice on regulatory issues; oversees the preparation of regulatory submissions; and assists with the development of regulatory strategies. She has excellent awareness and a clear understanding of local requirements across Europe and CIS region.
Martynas Juzenas, MPharmMartynas Juzenas has over 10 years of experience in pharmaceutical industry, with key areas of interest in Pharmacovigilance, Clinical Safety, Regulatory Affairs and Quality Assurance. Martynas has joined CRO Biomapas in 2007 and since then he has dedicated his expertise and skills to the establishment and management of Pharmacovigilance Department. Martynas has highly contributed to the geographical expansion of Pharmacovigilance service as well as to the addition of new services, i.e. Clinical Safety, Medical Monitoring. He is also an internal auditor at Biomapas since 2011. Martynas holds a master degree in Pharmacy.
RA and PV Manager, CIS
Aliaksandr Bakshtanovich, MDAliaksandr Bakshtanovich has joined Biomapas as a Regulatory Affairs and Pharmacovigilance Manager for the former CIS Region. He has over 5 years of experience in pharmacovigilance as PV Manager in top pharma company in Belarus as well as a clinical pharmacologist in Minsk Hospital. Holding the last position, he collaborated with Belarus Health Authorities in the frame of local PV projects dedicated to in-patient hospitalization due to Adverse Drug Reactions. Apart from PV, he has gained Quality Management System related expertise while holding a position as a Local Quality Responsible Person. Aliaksandr is a medical doctor by training.
Country Manager, Switzerland
Lukas Sveikata, MDLukas Sveikata as a Country Manager of Biomaps CRO office in Switzerland is responsible for operational processes and business development. After obtaining a Medical Doctor degree in Lithuania, Lukas is currently finishing his post-graduate training in clinical neurology in Switzerland. His interests lies in clinical research in neurology and neurorehabilitation, good governance in healthcare and drug development.
Country Manager, Georgia
Ioseb Qureli, MD, PhDIoseb Qureli as Country Manager/Director of CRO Biomapas office in Georgia is responsible for the operational processes and team management. He has over 30 years of experience in medicine, science and clinical research. Ioseb held different scientific positions in Scientific Research Institution, also performed administrative tasks as a Head of Pathomorphological Department and as a Head of the Center of Clinical Diagnostics. At the same time, he worked as the associated professor in several medical universities and colleges in Georgia. Ioseb is a co-author of 12 scientific publications. He is a clinical research expert with over 10 years of experience in the field. His main activities include study start-up management, regulatory affairs of clinical trials, site selection and clinical monitoring, GCP and local regulation advise, negotiation with vendors, staff management. Ioseb is a medical doctor by training and holds a PhD in the field of pathology.
Country Manager, Russia
Elgudzha Kutidze, MD
Country Manager, Ukraine
Olena Udovichenko, MD
Clinical Research Assistant
Biomapas offers a great career opportunity - we are looking for proactive person to join our team as Clinical Research Assistant
Regulatory Affairs Specialist
Biomapas is looking for pro-active person with creative approach to join our growing team as a Regulatory Affairs specialist. This position requires good communication skills and fit to a person who is confident enough to manage a lot of ongoing projects.
More information will be available soon. For a job description please contact email@example.com