Clinical Trials

We provide full-service solutions for Phase I-IV clinical research and medical devices. We have clinical experts in over 20 countries and experience in the following therapeutic areas: oncology, CNS, cardiovascular, infectious disease, immunology, rheumatology, pulmonology, endocrinology, gynecology, gastroenterology, nephrology, ophthalmology, urology and dermatology.

Early Phase Unit (Lithuania)

 
BIO1 is Biomapas’ early phase unit located in Lithuania’s leading university hospital-Vilnius University Hospital, Santaros Clinics (≈1400 beds). 

Reasons for customers selecting BIO1 include the following: 

  • Excellent environment for patient recruitment due to investigators being financially and scientifically motivated, and where there is generally easy access to patients and healthy volunteers;
  • Ethics committee time to approval is approximately 1-2 months;
  • Strong partnerships and cooperation with key opinion leaders in a wide range of therapeutic areas who can bring their expertise to protocol development, clinical conduct and data analysis;
  • The hospital’s ICU is in the same building;
  • The BIO1 team has particular expertise in oncology, cardiology, dermatology and gastroenterology;
  • The unit has 12 beds and is already appointed to expand to 20 beds if needed;
  • The facility offers a large clinical space of 500 m2 plus an administrative area of 120 m2 – all of which is modern, immaculate and has the very latest equipment.

BIO1 offers a safe and comfortable environment for patients or healthy volunteers.  It provides each  customer with a project manager as a principal point of contact who oversees the whole process from recruitment to clinical study reports.

The facility covers all types of early phase clinical studies, including first-in-human and proof-of-concept, single and multiple doses, bioequivalence, bioavailability, drug-drug and drug-food interaction, PK/PD, tQTc studies. 

Additional services include:

  • Protocol writing;
  • CTA submissions and Competent Authority/Ethics Committee approvals;
  • CRF Design;
  • Recruitment of Patients or Healthy Volunteers;
  • Monitoring;
  • Quality Assurance;
  • Data Management;
  • Centralized laboratory;
  • ICU Access;
  • PK Analysis;
  • Statistical Analysis;
  • Clinical Study Report.

For any inquiry regarding our services, please contact Biomapas Business Development team.

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