Clinical trials, Pharmacovigilance, Regulatory AffairsBiomapas is a privately owned contract research organization (CRO), established in 2001. We have solid experience in numerous therapeutic fields such as, but not limited to, psychiatry, cardiovascular, oncology, neurology, rheumatology, pulmonology.
We also have a long history of cooperation with the Lithuanian University of Health Sciences, University Clinics and other Lithuanian medical institutions. Biomapas has the capability of conducting Phase I-IV clinical trials including bioequivalence (PK/PD) studies for the pharmaceutical and biotechnology industries, as shown by our continuing success.
We are committed to customer service and satisfaction. We bring to our business partnerships the flexibility and adaptability of a small, team centred company. Those teams have a very low staff turnover and consist of experienced clinical research professionals with medical and healthcare backgrounds.
All these strengths allow us to help our customers with state of the art solutions from early phase research all the way up to final product registration. Our regulatory affairs team is experienced in providing a full range of regulatory affairs solutions and is geared to delivering the highest quality support, in achieving approval for your medicine pipeline in a timely and cost-effective manner.
Our quality is supervised by our internal Quality Management System which is ISO 9001 certified. Our integrity is supported by being the CA authorised GCP trainers in Lithuania.
Project timelines, cost and quality management are our core priorities when addressing our customers’ needs.