Clinical studies are organised for the development of biological and medical knowledge aimed at improving health in humans. Such studies or clinical trials involve several phases (I-II-III-VI or post-marketing).
Conducting a survey requires the collection of a large amount of data that can be entered, checked, confirmed and finally grouped together in a single database. These steps require significant logistical means in order to comply with the GCP(Good Clinical Practice) and regulations on the protection of people's safety and well-being.
The setting up of a central database and an electronic collection form via the Internet called e-CRF (electronic Case Report Form) meets these needs by combining technology, simplicity, privacy and data security.
Data entry online:
The use of e-CRF can be a means to aid and accelerate the implementation of programs for pharmaceutical and clinical development and significantly reduce the logistics and study costs.
The advantages of e-CRF vs. Paper CRF:
Learn more :
EOL New brochure available!
March 2016 : EOL the new brochure is available!
Medsharing in figures
(Figures 2024)
280 000 patients since 2003 for over 320 studies.
70 Registries / Observatories.
99 Interventional studies.
162 non-interventional studies.
includes :
37 IWRS (without eCRF)
92 Medical device studies
110 Drug studies
116 Surveys / Assessments
89 Ongoing studies.
Figures 2024
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