Unlock efficiency and collaboration with Cloudbyz's truly Unified eClinical Trial Management Platform. From CTMS to Safety & PV, streamline your trials for faster, compliant outcomes.
“Veeva eTMF helps us maximize clinical trial efficiency and strengthen our partnerships to accelerate the delivery of treatments to patients.” Nigel Blackburn, Director of Drug Development Cancer Research UK Read press release “We now have rich insights about our clinical process, affording Merck ...
Clinical OneClinicalTrial Platform The OneClinicalTrial Platform is an Integrated Digital Clinical Trial Platform which enables Sponsors, CROs, and Research Sites work collaboratively and manage all aspects of clinical trials effectively in one place. Read More Master Data Management (MDM) Clinevo Ma...
Protocol-Centricity in Modern Clinical Trials: Striking the Right Balance Read More Octalsoft’s MD Hiren Thakkar Joins Esteemed Panel at ISCR 18th Annual Conference Read More Empowering Pharma Clinical Trials: Octalsoft’s ePRO Solution for Phase 3 COVID-19 Research Read More Top Clinical ...
Solutions division, stated, “We’re very proud that INC Research has chosen Trial Interactive as its eTMF solution. INC’s global reach and commitment to utilizing technology should only serve to benefit their study sponsors as they seek to become more efficient in conducting global ...
UroGen Pharma streamlines clinical and regulatory operations Watch demo Quickly transfer TMF documents and eliminate end-of-study migrations Watch demo Process documents quickly and increase quality with the TMF Bot Watch demo Gain important information about inspection readiness on the Veeva eTMF homepage...
Veeva Vault eTMF is the leading trial master file application used to ensure the quality, timeliness, and completeness of a TMF. Enterprise content management capabilities It provides full enterprise content management capabilities for upload, version control, QC and approval, and real-time co-authorin...
documents have signature requirements based on regulations. Often, signatures are obtained because of an organizational policy, written or unwritten, not based on regulations. The UK Medicines and Healthcare Products Regulatory Agency (MHRA) reinforces this distinction in its 2012 Good Clinical Practices...
The eTMF Connect system can be used to empower clinical sites to contribute documentation to the TMF in a timely manner, increasing efficiency and timeliness along the way. Montrium’s site management functionality streamlines collaboration with clinical sites, institutions, and medical practices to ...
Clinical Research Suite Pricing Model 1: On Demand Pay As You Go Get a Cost Estimate within 1 minute ➞https://my-researchmanager.com/en/on-demand/ For fewer than 5 ongoing projects Perfect entry model with our pay-as-you-go plan. Transparent Pricing Matrix Pay-After-Use Billing Various...