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Data management
4Clinics Data Management team insures the rapid and accurate collection and cleaning of all kind of clinical data by collaborating closely with the different teams, in compliance with regulations, procedures and protocol-required information.
Pharmacovigilance
The 4Clinics safety team offers the support in the detection, the surveillance, the prevention and the assessment of adverse events collected on drugs, from the clinical trials to the post-marketing development.
Biostatistics
The 4Clinics biostatistics team is involved since the start of clinical trial to ensure the quality of study design, data analysis and reporting.
Medical & Scientific writing
Our team dedicated to medical writing can provide the full range of medical documents required during your clinical program.
Regulatory Affairs
For assistance with regulatory affairs you do not need to look further. Our team is highly-experienced and well-trained.
Scientific communications
Our team dedicated to scientific communications can provide scientific documents tailored to different audiences and media.
Data management
Pharmacovigilance
Biostatistics
Medical & Scientific writing
Regulatory Affairs
Scientific communications
DB Locks
CRF
CDA
RDC
Spass
CIOMS
Empiricatrace
Randomization
MedDRA
Clintrace
Medical Writing
Safety
Data Mapping
Regulatory
NSAE
EDC
ARIS
Power Calculations
Medical Review AE Reports
Sample Size
Compliance
Pharmacovigilance
Oracle Clinical
Biostatistics
Statistical Protocol
SAE
Statistical Report
Clintrial
ISS
PSURs
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