Ratings and Reviews 15 Ratings
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What is IQVIA?
Across the globe, various organizations turn to IQVIA to expedite the drug development journey, ensuring product safety and quality while improving commercial effectiveness, facilitating appropriate treatment access for patients, and ultimately driving better health outcomes through enhanced healthcare delivery. By adopting a modern approach to clinical development that incorporates data, technology, and analytics, you can streamline your trials effectively. The result? Faster decision-making processes and reduced risks, allowing for the faster introduction of groundbreaking therapies. Leveraging its deep industry expertise, extensive data, and advanced analytics, IQVIA provides customized solutions to a diverse range of clients within the healthcare sector. You can keep up with the latest findings and updates shared by IQVIA's experts, including data scientists, healthcare professionals, and researchers, on significant topics that align with your interests. From trending industry shifts to practical applications of innovative capabilities, a treasure trove of knowledge is available for your exploration. Engaging with this rich content not only keeps you informed but also equips you to navigate successfully in an ever-changing healthcare landscape, ensuring you are always one step ahead.
What is Clinion RTSM?
Clinion RTSM simplifies the management of clinical trial supplies and patient randomization through the use of Interactive Response Technologies (IWRS).
The Inventory module seamlessly connects with the Randomization module of Clinion RTSM Software, enabling the execution of both straightforward and intricate randomization strategies tailored to protocol requirements.
Recognized as one of the leading integrated EDC/RTSM platforms in the market, Clinion allows site users to manage randomization, drug allocation, returns, and reallocation without the need to log into multiple systems or concern themselves excessively with reconciliation.
Our straightforward and cost-effective pricing structure helps reduce the overall expenses associated with RTSM ownership, ensuring that quality and functionality are maintained.
By combining EDC and RTSM modules, you can enhance operational efficiency and maximize the benefits of your clinical trial management processes.
Integrations Supported
Clinion EDC
Cognipharma
DrugDev Spark
IQVIA RIM Smart
Own Data
Winpharm
Integrations Supported
Clinion EDC
Cognipharma
DrugDev Spark
IQVIA RIM Smart
Own Data
Winpharm
API Availability
Has API
API Availability
Has API
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Company Facts
Organization Name
IQVIA
Date Founded
1982
Company Location
United States
Company Website
www.iqvia.com
Company Facts
Organization Name
Clinion
Date Founded
2000
Company Location
India
Company Website
www.clinion.com/randomisation-and-trial-supply-management-software/
Categories and 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
Categories and 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