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Biovantix Resources

We at Biovantix aim to have the most appropriate human resources with the necessary expertise to make the Customer project a successful venture. We aim to provide our Customer with the most appropriate, qualified, experienced and skillful staff.

Our clinical structure employs people for the following positions: Project Manager (PM), Start-up and Regulatory Manager (SRM), Clinical Team Leader (CTL), Clinical Research Associate (CRA) and Clinical Trial Assistant (CTA).

All Biovantix people are excellently prepared in terms of education, training and experience and continuing personal development is amongst our top values. The Company ensures regular general and on-the-job trainings through organized training sessions, attendance of Sponsors’ and third parties’ organized trainings, co-monitoring activities, regular follow-up trainings, etc. Some of our staff are certified by the Association of Clinical Research Professionals (ACRP) and all of the staff are members of different professional organizations and associations. 100% of Biovantix staff are fluent in English, have profound computer literacy, perfect interpersonal communication abilities, open and friendly attitude and adhere to the best business practice standards.

The strict adherence of our personnel to the highest professional and ethical standards is constantly reinforced and assured through regular quality assurance activities and feedback from Customers and Investigators. We are in the firm belief that quality is a key factor for successful and profitable Customer and Investigator relations and also for the best welfare of trial subjects.

Efficiency is another value that is highly honored by Biovantix. We pay special attention to proper and efficient allocation of available and potential resources so that projects timelines, milestones and metrics are continuously met with the highest quality. For this we employ different approaches including appropriate human resourcing, activities automation using electronic systems, proper responsibilities delegation and subcontracting of additional resources and experts when necessary.

Key Project Experience

Our project experience includes large international trials which conduct in Bulgaria was/is done by us for leading pharmaceutical companies and CROs:

  • Cardiovascular Diseases: Acute ST-Elevation Myocardial Infarction (STEMI) – Phase IIIA; Acute Coronary Artery Syndrome – Phase IV / PMS; Acute Coronary Syndrome with early PCI – Phase II;

  • Orthopedics: Prevention of DVT in Total Hip and Knee Replacement Surigeries – Phase II;

  • Gastroenterology: Diarrhea Predominant Irritable Bowel Syndrome – Phase III;

  • Endocrinology: Diabetes Mellitus Type 2 – Phase IIIB/IV; Diabetes Mellitus Type 1 – Phase IV; Diabetes Mellitus – Observational Study; Growth Hormone Deficiency in Adults – Phase IIIA; Growth Hormone Deficiency in Children – Phase IIIA;

  • Allergy/Asthma and Pulmology: Perennial Allergic Rhinitis – Phase IIIA; Influenza in Asthmatic Children – Phase  IIIB; Cystic Fibrosis – Phase Ib/IIa;

  • Oncology: Breast Cancer – Phase III; Colon Carcinoma – Phase III;

  • CNS: Relapsing/Remitting Multiple Sclerosis – Phase II; Bipolar I Disorder – Phase III.


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