Patient Trial Management
Biotrial's Advantages for Patient Trial Management
Biotrial is a reliable and experienced full-service provider in Early Phase Trial Management. Being a mid-sized CRO in the Patient Trial Management field allows us to provide you a close partnership with our highly skilled, motivated and dedicated team members, fully adaptable to sponsor processes.
Key strengths of our services include: our commitment to deadlines, flexibility and the high quality standards we follow.
Working with Biotrial gives you access to:
- Scientific & Medical Expertise
- Technical Expertise
- Targeted Networks
Biotrial has the technical know-how and skilled staff to carry out all stages of your patient study projects:
- Protocol, CRF, ICF, IB Conception
- EC & Regulatory Submission
- Investigator meeting
- Hospital & Investigator Contract Management
- Patient Recruitment
- 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, 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 therapeutic expertise at every level of your study process.
For more information on our Patient Trial Management please contact us: firstname.lastname@example.org