EMSCO provides services including review of trial design, medical writing, support with essential clinical trial documents, contracts, publications, management and coordination of clinical trials and projects associated with MDS. EMSCO’s multilingual staff has ample experience in the international context and is therefore apt to fulfil these tasks.
One of the major goals of EMSCO is to offer an expert MDS office team to assist, design and review clinical trials in MDS. The team includes a lead KOL, a biostatistician, data collection personnel and management personnel. Furthermore, standardized Clinical Trial Documents and SOPs for MDS trials are created. One of the main goals of EMSCO is to improve the quality and comparability of clinical trials.
- Sponsor Function (with GMIHO as legal representative
- Site recruiting / feasibility
- Essential trial documents (protocol, regulatory submission)
- Medical Writing
- MDS specific eCRFs and SOPs
- Data Management