|Clinevo Technologies Pvt Ltd|
We are 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. Clinevotech software solutions company specialized in clinical trials, data warehousing, drug safety , eTMF (electronic trial master file) for Pharma, Pharmacovigilance, Biotech, life sciences and CROs in Bangalore, India, USA, Europe
Clinevo electronic Trial Master File (eTMF) is an easy to use electronic Trial Master File in electronic (digital content) format for organizing and storing documents, images, and other digital content of clinical trials. Clinevo electronic Trial Master File (eTMF) has inbuilt DIA reference model and meets regulatory guidelines including: Digital Content Archiving, Security and Access Control, Change Controls, Audit Trails and System Validation
Clinevo Clinical Trial Management System (CTMS) meets the regulatory guidelines including security, access control, change controls, audit trails, and the best system validation. A Clinical Trial Management System (CTMS) is a software application that supports the Clinical trial processes. It provides infrastructure, consisting of three components: Clinical Data Management System (CDMS), Site Management System (SMS), and a Patient Recruitment Database or a Clinical Trial Web Portal that enable a site to plan, implement, monitor, analyze and report on clinical research activities to maximize the probability of delivering high-quality data within time and budget constraints.