MDS Finland provides CRO-Services for the pharmaceutical and medical device industries. The main role of CRO-Services is to help sponsors to plan, coordinate, implement, and supervise the processes that are involved in a clinical investigation according to the national laws and international standards. CRO-Services are also the main contact point between the sponsor, authorities, and study site. CRO-Services ensures clinical investigation quality and compliance according to ICH-GCP and ISO 14155 -standard.

MDS FinlandĀ“s CRO-Services include all those assignments that sponsor wants to outsource related to clinical investigations.

Digital operating environment

MDS Finland recommends sponsors to use EDC (Electronic Data Capture) during a clinical investigation. MDS Finland helps setting up a relevant electronic database for the clinical investigation. MDS Finland helps in EDC use, develops customized data status reports, and performs data reviews and cleaning. With help of EDC, sponsor can follow-up realtime clinical data status. EDC makes clinical data review, monitoring, quality control and reporting easier and quicker for the sponsors and CRO personnel.