Our Services Clinical Trial Management Phases II-IV Bioequivalence/bioavailability Data Management Database design Data management/independent double data entry Data query management Statistics Trial design and sample size calculation SAS programming Statistical analysis Medical Writing Investigator's Brochure Protocol and CRF development Patient information and Informed consent form Integrated study reports Periodic safety update reports Clinical summaries Analytical Services Analytical method development/validation Bioanalysis Regulatory Services Regulatory consulting Preparation/submission of registration dossiers Contract Staff Our Experience Oncology Hematology CNS Metabolism Cardiovascular Pharmacokinetics Our Benefits Accessible patient populations Fast recruitment Excellent patient compliance and reduced drop-out rate Highly trained and motivated investigators Investigator sites - high quality specialized hospitals Drug legislation fully harmonized with the inthernational standards Cost effectiveness Contact us 55A, Bulgaria Blvd., 1404 Sofia, Bulgaria Tel.: +359 2 958 95 17; +359 2 958 95 18 Fax: +359 2 958 68 22 E-mail: meditrial@medtr-bg.com Web: www.medtr-bg.com
medtr-bg.com
Please
click here
to view the non-framed version.