Global Electronic Trial Master Market Companies
The key players operating in the market include, Veeva Systems Inc., Oracle, GiantFocal, and others. These key players are leveraging several key strategies, including focusing on cloud-based solutions, emphasizing improved efficiency and regulatory compliance, and partnering with CROs. These strategies are aimed at increasing the adoption of eTMF systems in the pharmaceutical and biotechnology industries, for driving electronic trial master file market growth.
List of Key Players in the Market:
- Veeva Systems Inc.
- Oracle
- GiantFocal
- Ennov
- TransPerfect Life Sciences
- MasterControl Solutions, Inc.
- SureClinical Inc.
- Aurea, Inc.
- Clinevo Technologies
- Montrium Inc.
- Anju Software, Inc.
- Cloudbyz
- Octalsoft
- Egnyte, Inc.
- IQVIA Inc.
Recent News:
- A prominent supplier of cutting-edge clinical trial solutions, EDETEK, announced the launch of CONFORM eClinical Version 5.1., in May 2024. A completely integrated suite of components was provided in this most recent edition with the goal of improving and streamlining the clinical trial management procedure. End-to-end, fully integrated components such as Electronic Data Capture (EDC), Randomisation and Trial Supply Management (RTSM), Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), Pharmacovigilance/Safety (PV/Safety), electronic Diary (eDiary), electronic Patient-Reported Outcomes (ePRO), electronic Clinical Outcome Assessment (eCOA), ePayment, and eConsent are all included in CONFORM eClinical Version 5.1. Data visualisation components, central and risk-based monitoring, and comprehensive Study Management are also included.
- Anju declared the launch of a new cloud-based electronic trial master file software program called eTMF Master, in June 2022. The technology makes it easier for sponsors, CROs, and sites to work together to safely and effectively manage clinical trial information in a setting that complies with regulations. Faster compilation of digital records and photos from clinical trials was made possible by eTMF Master in order to satisfy growing regulatory requirements and timelines for internal audits, sponsor audits, and agency inspections.
- LifeSphere Extended Clinical Collaboration Electronic Trial Master File (eTMF) System. The majority of medical advancements were the result of collaboration, in April 2021. But all too frequently, poor clinical information management can make collaboration challenging. For example, when clinical research sites are forced to use proprietary solutions in order to satisfy partner demands, they suffer. In actuality, the disorganised quantity of programs and outdated IT infrastructure make clinical work difficult for all parties concerned. This is not only extremely unproductive, but it is also annoying.