Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
In recent years, the Life Sciences sector has incurred nearly $15 billion in fines and settlements related to compliance, underscoring the importance for firms to follow best practices in pharmaceuticals, medical devices, and biotechnology. Additionally, the way clinical trials are managed can greatly influence the timeline, scope, and financial resources allocated for the development of drugs or medical devices. Utilizing OpenText™ Clinical Trial Quality Management System (ctQMS) allows organizations to maintain compliance, lower record management expenses, and foster collaboration to implement best practices throughout the entire clinical trial lifecycle. This strategic approach not only enhances operational efficiency but also contributes to the overall success of product development initiatives.
Description
Discover the innovative validation solution designed to automate, unify, and expedite your achievements. Res_Q assists IT and quality leaders in eliminating validation debt, ensuring tranquility, and allocating valuable resources effectively. With its data-centric architecture and extensive range of applications supported by various industries, Res_Q prevents you from deepening your validation debt with each new software release. The open API framework facilitates a bi-directional data exchange, which enhances system integrations and streamlines migration during the onboarding process. Tailored workflows are available to align with your operational needs while incorporating industry best practices seamlessly. Every validation procedure is managed within a unified system that caters to all sectors of the organization, such as IT, manufacturing, lab systems, and beyond. You can initiate workflows and delegate tasks based on the risk profile, ensuring that quality remains a priority without compromising on speed. By leveraging Res_Q, organizations can enhance their operational efficiency and foster a culture of continuous improvement.
API Access
Has API
No
API Access
Has API
Yes
Screenshots View All
No images available
Integrations
Adobe Acrobat Sign
No
Amazon Web Services (AWS)
No
Benchling
No
Box
No
Docusign
No
LabVantage
No
LabWare LIMS
No
MasterControl
No
Microsoft Dynamics 365
No
NetSuite
No
Integrations
Adobe Acrobat Sign
Yes
Amazon Web Services (AWS)
Yes
Benchling
Yes
Box
Yes
Docusign
Yes
LabVantage
Yes
LabWare LIMS
Yes
MasterControl
Yes
Microsoft Dynamics 365
Yes
NetSuite
Yes
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Customer Support
Business Hours
No
Live Rep (24/7)
No
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
No
In Person
No
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
No
Vendor Details
Company Name
OpenText
Founded
1991
Country
Canada
Website
www.opentext.com/info/clinical-trial-management
Vendor Details
Company Name
Sware
Country
United States
Website
www.sware.com/solutions/platform
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
No
Document Management
No
Electronic Data Capture
No
Enrollment Management
No
HIPAA Compliant
No
Monitoring
No
Patient Database
No
Recruiting Management
No
Scheduling
No
Study Planning
No