Presentation

Biotrial's advantages for Oncology Trials

Biotrial is a reliable and experienced full-service provider in Oncology trials. Being a mid-sized CRO in the Oncology field allows us to provide you a close partnership with our highly-skilled, motivated and dedicated team members, fully adaptable to sponsor processes. Cornerstones of our services are also our commitment to deadlines, flexibility and the high quality standards we follow.

Working with Biotrial gives you specific access to:

• Scientific & Medical Expertise 
• Technical Expertise 
• Targeted Networks

Experience

Biotrial has an extensive experience in clinical trial management including multicentric & Pharmacokinetics/ Pharmacodynamics oncology studies.

• Phase I
  • Pharmacokinetic
  • Pharmacodynamics
  • Food Interaction
  • ADME

• Phase II-IV
  • Cytotoxics
  • Hormonotherapy/Immunotherapy
  • Hematopoietic Growth Factors
  • Targeted Drugs

Services

Biotrial has the technical know-how and skilled staff to carry out all stages of clinical trials:

• Feasibility
• Protocol, CRF, ICF, IB Conception
• EC & Regulatory Submission
• Investigator Meetings
• Hospital & Investigator Contract Management 
• Coordination (Newsletters, regular reports…)
• Monitoring
• SAE Management
• SMO, Central Laboratory, Centralized ECG, MRI
• Data Management & Biostatistics
• Quality Assurance 
• Clinical Report

Staff

Our highly-qualified staff of CRAs, Project Managers, Study Assistants, study Nurses & Technicians, Data Managers, Biostatisticians, Medical Writers and Quality Assurance Officers are fully dedicated to your projects. Annually trained on ICH GCP, Clinical trial procedures, regulatory questions as well as on specific pathologies, our team provides in-depth oncology expertise at every level of your study process.

For more information please contact us:
contact@biotrial.com