Press release
Electronic Trial Master File (eTMF) Market Expected to Expand at a Steady CAGR through 2026
Electronic Trial Master File (eTMF) Market: Drivers and Challenges
Life sciences companies that engage in clinical trials are required to document the important issues of the trials. The trial documents facilitates the conduct of clinical trials, and prove the quality data produced. The various governments across the world requires that trial documents filed and maintained in both the trial sponsor and the tester file. Now-a-days, according to various government’s requirements, the final close-out of a trial can only be accomplished when the medical site monitor has reviewed and confirmed that all necessary documents are in the suitable folder.
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Due to these strong reporting requirements, sponsors are often tangled in internal and regulatory audits for discrepancies in the trial master file. On numerous occasion, required documents are missing at either the sponsor or trial site. Because of these complexity involved in manual documentation, there is a requirement of electronics trial master file (eTMF) processes.
Electronic Trial Master File (eTMF) Market: Segmentation
Segmentation on the basis of component:
Software
Services
Segmentation on the basis of deployment:
On-premises
SaaS
Segmentation on the basis of end-user:
Pharmaceutical Companies
Contract Research Organization
Life Science Organization
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Electronic Trial Master File (eTMF) Market: Competition Landscape
Few of the companies in eTMF market are: SureClinical Inc., Montrium Inc., TransPerfect Trial Interactive, Veeva Systems, Phlexglobal Ltd, Paragon Solutions, Mastercontrol, Inc., Wingspan Technology, Inc., Arivis AG, Biovia (QUMAS), Ennov, Database Integrations, and PharmaVigilant I-Vault.
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