Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
Res_Q is an AI-powered electronic validation platform designed to help life sciences organizations manage computerized system validation and regulatory compliance. Developed by Sware, the cloud-based software centralizes validation planning, documentation, execution, approvals, and ongoing lifecycle management. Its agentic AI capabilities automate administrative activities, monitor validation progress, and identify milestones that require review or intervention. Intelligent risk assessment tools evaluate system criticality to prioritize validation workloads and support risk-based compliance strategies. The platform includes automated document processing that converts uploaded validation materials, vendor manuals, and supporting records into organized, searchable information. Its video-to-script functionality transforms recorded software processes into structured validation test scripts. Smart dashboards provide visibility into validation status, operational performance, outstanding tasks, and compliance activities across multiple systems and locations. Res_Q supports GCP, GLP, GMP, and AI validation workflows, including risk-based documentation and change management aligned with GAMP 5 principles. Through Res_Q Connect, organizations can integrate applications such as Jira and ServiceNow, coordinate automated testing, and maintain audit trails across connected systems.
Description
Transform your Life Sciences operations by significantly enhancing the control, efficiency, and quality of your products and processes. Maintain inspection readiness consistently with our fully compliant platform, which has undergone pre-validation in line with GAMP5 standards. Gain complete oversight of your processes and documentation, allowing for perfectly customized workflows and maximized automation wherever feasible. Experience smooth operations and comprehensive traceability through our seamlessly connected modules. Our committed team is available to address any inquiries you may have at any moment. Only the finest Scilife experience meets our high standards! The Scilife platform not only streamlines but also automates and organizes every aspect of your industry, whether in Medical Devices, Pharma & Biotech, or ATMP. Click below to explore the specific Scilife modules that cater to the distinct lifecycle stages within your industry. Our software is not just equipped with all the essential quality tools you would anticipate; it also comes with numerous additional features that surpass expectations, ensuring your operations thrive. We're excited to partner with you on this transformative journey!
API Access
Has API
Yes
API Access
Has API
No
Integrations
Adobe Acrobat Sign
Yes
Amazon Web Services (AWS)
Yes
AuthPoint
No
Benchling
Yes
Box
Yes
Docusign
Yes
LabWare LIMS
Yes
MasterControl
Yes
Microsoft Azure
No
Microsoft Dynamics 365
Yes
Integrations
Adobe Acrobat Sign
No
Amazon Web Services (AWS)
No
AuthPoint
Yes
Benchling
No
Box
No
Docusign
No
LabWare LIMS
No
MasterControl
No
Microsoft Azure
Yes
Microsoft Dynamics 365
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Pricing Details
$1000
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
No
Live Rep (24/7)
No
Online Support
Yes
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
No
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
No
Vendor Details
Company Name
Sware
Founded
2015
Country
United States
Website
www.sware.com/products/res_q
Vendor Details
Company Name
Scilife
Founded
2017
Country
Belgium
Website
www.scilife.io
Product Features
Product Features
Quality Management
Audit Management
No
Complaint Management
Yes
Compliance Management
No
Corrective and Preventive Actions (CAPA)
Yes
Defect Tracking
Yes
Document Control
Yes
Equipment Management
Yes
ISO Standards Management
No
Maintenance Management
Yes
Risk Management
No
Supplier Quality Control
No
Training Management
Yes