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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 CASQ-it?

Ensuring that business processes are devoid of defects leads to the production of flawless products. This is the fundamental reason CASQ-it was created to encompass every aspect of your quality assurance and management protocols, starting from the development phase and extending through material handling to supporting processes. The true strength of CASQ-it lies in its process-oriented methodology, which includes a feature that permits your CAQ system to adapt effortlessly to your unique workflows instead of compelling your operations to adjust to it. By facilitating this adaptability, CASQ-it sets the stage for your quality assurance initiatives to evolve, thereby enhancing quality and reliability, which ultimately increases customer satisfaction and reduces costs associated with quality issues. Each module within CASQ-it functions autonomously, allowing for the rapid optimization of specific processes and workflows throughout your organization. Furthermore, these modules can be integrated in numerous configurations or employed to create a comprehensive quality assurance system designed for your specific requirements. This level of adaptability not only supports ongoing improvements but also encourages innovation in your quality management practices, ensuring your organization remains competitive in an ever-changing market. Ultimately, investing in CASQ-it means committing to a future where quality excellence is not only achievable but sustainable.

Media

Media

Integrations Supported

AuthPoint
Microsoft Azure
Microsoft Excel

Integrations Supported

AuthPoint
Microsoft Azure
Microsoft Excel

API Availability

Has API

API Availability

Has API

Pricing Information

$1000
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

Scilife

Date Founded

2017

Company Location

Belgium

Company Website

www.scilife.io

Company Facts

Organization Name

BÖHME & WEIHS

Date Founded

1985

Company Location

Germany

Company Website

www.boehme-weihs.de/en/

Categories and Features

Quality Management

Audit Management
Complaint Management
Compliance Management
Corrective and Preventive Actions (CAPA)
Defect Tracking
Document Control
Equipment Management
ISO Standards Management
Maintenance Management
Risk Management
Supplier Quality Control
Training Management

Categories and Features

Audit

Alerts / Notifications
Audit Planning
Compliance Management
Dashboard
Exceptions Management
Forms Management
Issue Management
Mobile Access
Multi-Year Planning
Risk Assessment
Workflow Management

Quality Management

Audit Management
Complaint Management
Compliance Management
Corrective and Preventive Actions (CAPA)
Defect Tracking
Document Control
Equipment Management
ISO Standards Management
Maintenance Management
Risk Management
Supplier Quality Control
Training Management

SPC

Corrective Actions (CAPA)
Data Entry
Data Linking
Data Management
Excel Loader
Job Management
OPC Data Collection
Performance Metrics
Point-of-Production Analysis
Real Time Data Collection
Regulatory Compliance

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