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Description
Scilligence's Scientific Data Management System (SDMS) offers a unified data storage platform that can connect with numerous instruments and devices, enabling researchers to quickly and securely access essential information. The automation features of SDMS facilitate the collection of data from scientific tools, equipment, or devices, and the subsequent extraction of metadata into a relational database, which enhances data management efficiency and promotes cost reduction. Our system ensures rigorous version control, comprehensive audit trails, and a detailed history of document changes that comply with prevalent regulatory standards. Furthermore, SDMS not only integrates effortlessly with Scilligence applications but also works harmoniously with laboratory instruments and devices for automated data collection. Additionally, it supports the integration of various other database systems and storage options. To safeguard your intellectual property, we provide robust access management at the site, account, and project levels, ensuring that sensitive information remains protected while facilitating collaborative research efforts. This comprehensive approach to data management ultimately empowers scientists to focus on their research while relying on a secure and efficient data infrastructure.
Description
Enhance the efficiency of regulatory operations within your organization to bolster compliance and facilitate research advancements. Veeva SiteVault simplifies the process of managing clinical trials by integrating your regulatory tasks, leading to improved effectiveness and adherence to regulations. You can oversee regulatory and source documents through a unified platform that complies with 21 CFR Part 11 and HIPAA standards. With real-time insights across all trials, SiteVault Enterprise boosts operational effectiveness, accelerates study initiation, and fosters swift, high-quality trial management. Transition away from manual workflows and customize your own processes to enhance both quality and speed in study activation. By granting monitors secure, direct access to your regulatory and source documents, you eliminate the hassles of EMR access and document redaction. Furthermore, you can tailor your workflows, generate reports, and create dashboards to gain deeper insights into start-up timelines and regulatory workflows, ultimately driving better outcomes for your clinical trials. This comprehensive approach not only streamlines processes but also enhances collaboration across teams.
API Access
Has API
API Access
Has API
Integrations
Microsoft 365
Pricing Details
No price information available.
Free Trial
Free Version
Pricing Details
No price information available.
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
Scilligence
Founded
2010
Country
United States
Website
scilligence.com/scilligence-sdms/
Vendor Details
Company Name
Veeva Systems
Country
United States
Website
sites.veeva.com/products/sitevault-enterprise/
Product Features
Scientific Data Management System (SDMS)
Analytics
Artificial Intelligence (AI)
Audit
Centralized Data Repository
Collaboration
Compliance
Data Security
ELN Integration
LIMS Integration
Workflows
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning
Scientific Data Management System (SDMS)
Analytics
Artificial Intelligence (AI)
Audit
Centralized Data Repository
Collaboration
Compliance
Data Security
ELN Integration
LIMS Integration
Workflows