Startup Services

Study Planning
SSS International Clinical Research can provide input for study design and protocol development early in the planning stages of a clinical program. This includes evaluation of sample size based on expected clinical findings and historical data. Input can also be provided with respect to the design of case report forms and computerized databases to ensure that data is optimally collected and organized. Randomization procedures matching the requirements of the study protocol can be developed.

CRF Design
SSS International Clinical Research can provide input with respect to the design of Case Report Forms (CRFs) and computerized databases to ensure that data is optimally collected and organized. We are experienced in all major indications and know how to design perfect questionnaires to optimize handling and paper flow. SSS International Clinical Research can care for printing the necessary number of hardcopies (NCR paper) and deliver them directly to the study sites.

Site Selection
SSS International Clinical Research can assist clients in the selection of GCP experienced investigators and can make recommendations based upon past experience. A particular asset of SSS International Clinical Research is its record of interaction with investigators. We have worked with and are maintaining contacts with investigators at reputable medical institutions and as well as with investigators on a specialist or GP level. SSS International Clinical Research can perform all tasks necessary to implement a Clinical Trial.

Submissions to EC and Authorities
The medical and monitoring staff has extensive experience interacting with investigators to finalize contracts and to expedite EC approval. We can assist in preparing all documents necessary to implement and perform a Clinical Trial, including informed consent forms, case report forms, administrative reports, operation manuals. SSS International Clinical Research GmbH usually submits the necessary documents to the federal and state authorities.