Clinevo Technologies is a Life Sciences IT company serving more than 50+ Pharma /CROs across the globe who do submissions to USFDA, EMA, etc. using our products. Our products and solutions comply with regulatory guidelines including ICH, GxP, 21 CFR Part11, Annex 11, GDPR, etc.,
Our Solutions:
CLINICAL
SAFETY
QUALITY
Electronic Data Capture (EDC)
Pharmacovigilance Database (PV)
Quality Management - CAPA, CR, Deviations, and Audits
Clinical Trial Management System (CTMS)
MICC Intake (PQCs, MIs, and AEs)
Document Management System (DMS)
Electronic Trial Master File (eTMF)
Website Case Intake (PQCs, MIs, and AEs)
Training Management System /eLearn
Remote monitoring (rSDV),
Electronic Investigator Site File (eISF)
MDM (Master Data Management)
MDR (Meta Data Repository)
Phone
8838925976
Location
B-203M, KSSIDC Complex III Block - 1st Floor, Elec Bangalore, India