Biotrial's Advantages for Oncology Trials
By working closely with a network of specialized researchers and clinicians, Biotrial offers a customized approach to Oncology development.
Our dedicated experts work together to provide guidance from Non-Clinical, in vitro & in vivo, through to Early Phase patient studies by building packaged services tailored to sponsor needs. With experienced project coordinators, Biotrial is present every step of the way to accompany clients through this important stage of their product development.
Working with Biotrial gives you specific access to:
- Scientific & Medical Expertise
- Technical Expertise
- Targeted Networks
Biotrial has an extensive experience in clinical trial management including multicentric & Pharmacokinetics/ Pharmacodynamics oncology studies.
- Phase I
- Food Interaction
- Phase II-IV
- Hematopoietic Growth Factors
- Targeted Drugs
Biotrial has the technical know-how and skilled staff to carry out all stages of clinical trials:
- Protocol, CRF, ICF, IB Conception
- EC & Regulatory Submission
- Investigator Meetings
- Hospital & Investigator Contract Management
- Coordination (Newsletters, regular reports…)
- SAE Management
- SMO, Central Laboratory, Centralized ECG, MRI
- Data Management & Biostatistics
- Quality Assurance
- Clinical Report
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: firstname.lastname@example.org