 | Feasibility surveys
|
| Selection and recruitment of study centers
|
| Clinical Study Applications, CTA
|
| Submissions to Ethic Committees
|
| Selection and coordination of the central laboratory
|
| Selection and coordination of further services
|
| Creation and maintenance of the Study Master File
|
| Creation of Investigators' Files
|
| Initiation of study centers
|
| Training of investigators and study nurses
|
| Organization of Investigator Meetings
|
| Patient recruitment support
|
| Monitoring / Site Management
|
| Management of study medication and material
|
| Query Management
|
| AE/SAE documentation
|
| Closing of the study centers
|
| Project management
|
| Project administration
|
| Insourcing / on-site support from our staff |
