Our services
Contact Research Organization (CRO)
SMS-oncology is a Contact Research Organization (CRO) that provides professional services for oncology clinical trials, from writing development plans to clinical study report writing. Our services include:
- Product development plan writing, including pre-marketing and launch strategies
- Protocol writing
- Feasibility studies
- Site selection, investigator recruitment & patient accrual (sites are pre selected based on continued experience)
- Clinical trial applications (submission to and approval from competent authority, ethics committee, and sites)
- Project management of trials
- Site monitoring
- (e)Data management
- Medical monitoring
- Clinical study report writing
- Medical writing, e.g. scientific papers, abstracts, and other publications
- General oncology and oncology drug development education
Our Clients
SMS-oncology’s services are typically of interest to:
- Biotech companies in oncology drug development.
- Clinical development departments of global healthcare companies involved in oncology, both at headquarters’ and local level.
- Oncology business units of global healthcare companies responsible for product launch and post marketing development.
Special Services for Non-EU Clients
For companies outside the European Union (EU), we can assist in achieving the requirements for starting clinical studies in Western EU and know the optimal routes to get your oncology study conducted there. Moreover, in case you do not have an EU-based office, we can assist in appointing a EU-based legal representative, which is a legal requirement in order for a clinical trial to commence in the EU.

