Clinevo Technologies is  a Software Development Company specialized in developing and implementing robust technology solutions for Life Sciences R&D. We help Pharma, Biotech and CROs in reducing their time and cost in Clinical trials by implementing innovative technologies that involves Data warehousing, Analytics, Collaboration, Automation, and Artificial Intelligence.

We are committed towards delivering the most efficient and practical end-to-end solutions with HIPAA, GXP, CSV, 21 CFR Part 11 and other applicable regulatory guidelines. Our unmatched domain experience and technology expertise enables us to deliver best solutions.

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)    

   

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