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What is Scilife?

Revolutionize your Life Sciences operations by greatly improving the control, efficiency, and overall quality of both your products and processes. With our fully compliant platform that has undergone pre-validation according to GAMP5 standards, you can consistently maintain inspection readiness. Achieve complete oversight of your processes and documentation, enabling perfectly tailored workflows and maximizing automation wherever possible. Enjoy seamless operations and extensive traceability through our interconnected modules that work in harmony. Our dedicated team is always on hand to respond to any inquiries you may have, ensuring you have the support you need. We are committed to delivering an exceptional Scilife experience that aligns with our high standards! The Scilife platform not only simplifies but also automates and organizes every element of your industry, whether it pertains to Medical Devices, Pharma & Biotech, or ATMP. Click below to discover the specific Scilife modules designed to address the unique lifecycle stages relevant to your field. Our software is fully outfitted with all the crucial quality tools you would expect, along with a host of additional features that exceed your expectations, empowering your operations to flourish. Join us on this exciting journey of transformation, and let’s elevate your capabilities together!

What is Res_Q?

Res_Q is an AI-powered GxP electronic validation and compliance management platform developed by Sware for pharmaceutical, biotechnology, and other regulated life sciences organizations. The software provides a centralized cloud-based environment for managing computerized system validation activities throughout the application lifecycle. Its validation management capabilities support planning, documentation, risk assessments, test execution, approvals, change management, and ongoing compliance monitoring. Agentic AI functionality automates routine administrative tasks, tracks validation progress, and identifies activities requiring review or human judgment. Intelligent risk scoring evaluates system criticality and other relevant factors to help quality teams prioritize validation activities and allocate resources. The platform includes automated asset processing that organizes uploaded vendor documentation, validation packages, protocols, and other supporting materials into searchable records. Its video-to-script feature converts recordings of on-screen software processes into structured validation scripts to simplify test documentation. Smart dashboards and analytics provide visibility into validation workloads, operational milestones, risk levels, and compliance status across departments and facilities. Res_Q supports validation requirements associated with Good Clinical Practice, Good Laboratory Practice, Good Manufacturing Practice, and artificial intelligence systems used in regulated environments. Its AI validation capabilities include risk-based documentation, change tracking, and performance monitoring aligned with GAMP 5 guidance and applicable regulatory expectations. Through Res_Q Connect, the platform integrates with enterprise applications, quality systems, and automated testing tools using governed workflows, approval controls, and traceable audit records.

Media

Media

Integrations Supported

AuthPoint
Microsoft Azure

Integrations Supported

Adobe Acrobat Sign
Amazon Web Services (AWS)
Box
Docusign
LabVantage
LabWare LIMS
MasterControl
Microsoft Dynamics 365
NetSuite
Nuvolo
Okta
OpenClinica
SAP Cloud Platform
Smartsheet
TraceLink
TrackWise
Veeva CRM
ZenQMS

API Availability

API Availability

Has API

Pricing Information

$1000

Pricing Information

Pricing not provided

Supported Platforms

SaaS

Supported Platforms

SaaS

Customer Service / Support

Standard Support
Web-Based Support

Customer Service / Support

Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training

Training Options

Documentation Hub
Webinars
Online Training

Company Facts

Organization Name

Scilife

Date Founded

2017

Company Location

Belgium

Company Website

www.scilife.io

Company Facts

Organization Name

Sware

Date Founded

2015

Company Location

United States

Company Website

www.sware.com/products/res_q

Categories and Features

Life Sciences

Not specified

Quality Management

Complaint Management
Corrective and Preventive Actions (CAPA)
Defect Tracking
Document Control
Equipment Management
Maintenance Management
Training Management

Categories and Features

Life Sciences

Not specified

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