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Description
Numerous organizations globally rely on IQVIA to accelerate the drug development process, guarantee the safety and quality of products, enhance commercial efficacy, deliver appropriate treatments to patients, and ultimately promote improved health outcomes by facilitating access to and delivery of healthcare. Transform your approach to clinical development by seamlessly integrating data, technology, and analytics to streamline your trials. The outcome? Quicker decision-making and minimized risks, enabling you to provide transformative therapies at a faster pace. With its expertise rooted in data, sophisticated analytics, and deep industry knowledge, IQVIA offers tailored capabilities to clients throughout the healthcare landscape. Stay informed by exploring the latest insights and updates from IQVIA's data scientists, healthcare professionals, researchers, and other industry experts on crucial topics that resonate with your interests. From emerging industry developments to practical applications of our capabilities, a wealth of information awaits you here. Engaging with this content also empowers you to stay ahead in a rapidly evolving healthcare environment.
Description
The successful evaluation of drug treatments and their protocols hinges on the effective gathering and sharing of thorough, timely, and high-quality data. To support this need, the Omda Compos suite of solutions is specifically crafted to enhance the management and effortless exchange of medical information across the clinical landscape. This innovative platform guarantees that users and applications involved in clinical trials and registries have easy access to vital data, fostering improved collaboration and effective data usage. At the heart of the Compos platform lies Omda Compos QR, which features a sophisticated database structure, data warehousing functions, user management, and other critical elements that uphold data integrity throughout the entire process, from collection to analysis. Maintaining streamlined user access and efficient logging practices is crucial for any clinical registry or trial. Within Omda Compos QR, user roles are defined to regulate access to designated sites, thereby enhancing security and control over the data management process. By prioritizing these features, the platform not only supports researchers but also improves the overall quality of clinical data handling.
API Access
Has API
API Access
Has API
Integrations
Cognipharma
DrugDev Spark
IQVIA RIM Smart
Own Data
Winpharm
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
IQVIA
Founded
1982
Country
United States
Website
www.iqvia.com
Vendor Details
Company Name
Omda
Founded
1999
Country
Norway
Website
omda.com/solutions/health-analytics/omda-compos/
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
Healthcare CRM
Audience Targeting
Campaign Management
Marketing Automation
Medical History Records
Patient Communications
Patient Management
Physician Management
Predictive Analytics
Patient Engagement
Appointment Scheduling
Care Planning
Collaboration
Messaging
Mobile Access
Patient Education
Patient Portal
Personal Health Record
Progress Tracking
Self Management