Our Clinical Research Services
From functional services to full-service oncology studies
As desired by our clients, SMS-oncology performs partial and full clinical research services.
SMS-oncology can perform all or several of the following activities for your clinical research study:
- Regulatory Submissions
- Data Management
- Biostatistics
- Feasibility
- Local Monitoring and Site Management
For early phase studies (phase I/II) our main competence is providing our full service package. Conducting early phase oncology trials requires flexibility, efficiency and determination. With one European location and our centralized small project teams existing of dedicated oncology professionals, we assure a focused and optimal execution of your study.
In summary, our services include:
- Protocol writing
- Biostatistics
- Feasibility studies
- Site and Investigator selection & Patient Accrual
- Regulatory Submissions (Competent Authority, Ethics Committee, and Sites)
- Project Management
- Site Monitoring
- Pharmacovigilance (Safety Recording and Reporting)
- Medical Monitoring
- (e)Data Management
- Clinical Study Report Writing
- Medical Writing (e.g. Scientific Papers, Abstracts, and Other Publications)
An oncology portal to bring investigators and sponsors together
SMS-oncology has developed a dedicated oncology study portal: www.study-portal.com/client-cases/. This study portal is a secure online platform which can be used by sponsors, investigators, SMS-oncology and patients. It facilitates mutual collaboration, online communication and document exchange. Its contents can be customized to fit a wide range of oncology study requirements, from online study management capabilities to handling of patient questionnaires.