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features
design
support

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Description

PROLab is a comprehensive software solution designed for the planning, organization, execution, and analysis of interlaboratory studies. It serves dual purposes: conducting proficiency tests to evaluate laboratory performance, in line with ISO 13528 standards, and facilitating collaborative studies that validate analytical methods, adhering to ISO 5725: 1‐6. This software is specifically equipped with features that fulfill the quality management and assurance standards outlined in ISO/IEC 17043 for proficiency testing providers. The validation process is thorough, incorporating both automated procedures and manual checks to guarantee the accuracy of reports, computations, and visual data presentations. Additionally, PROLab aligns with the statistical evaluation standards set forth in relevant guidelines, ensuring that data analysis meets required criteria. It also offers tools that aid in assessing laboratory performance across various proficiency testing rounds. Furthermore, the software allows for user-friendly data entry and management, with a versatile data import module simplifying the process. This flexibility enhances the overall efficiency and effectiveness of laboratory studies.

Description

QIS has gained traction among numerous clients globally, enhancing product uniformity, minimizing quality defects, streamlining process efficiency, and supplying essential data to boost performance in manufacturing settings. By streamlining the gathering, evaluation, and visualization of shop-floor data, QIS ensures comprehensive visibility of relevant, real-time information throughout the manufacturing cycle. This system empowers users to make swift decisions on the shop floor and equips them with analytical resources to pursue long-term strategic objectives. With its capability to provide improved visibility, access, and traceability of real-time quality metrics, QIS allows operators and quality assurance teams to act proactively and preventively, thus lowering the chances of product failures and reducing quality-related expenses. Additionally, QIS supports both manual and automated data collection, simplifying the process for operators to input and analyze in-line quality assessments alongside laboratory test outcomes, ultimately fostering a culture of continuous improvement. Furthermore, the implementation of QIS can lead to significant advancements in overall operational efficiency, encouraging a more responsive and agile manufacturing environment.

API Access

Has API No 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

Microsoft Excel Yes 

Integrations

Microsoft Excel No 

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 No 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows Yes 
Mac No 
Linux No 
Chromebook No 

Deployment

Web-Based No 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows Yes 
Mac No 
Linux No 
Chromebook No 

Customer Support

Business Hours Yes 
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 Yes 

Types of Training

Training Docs Yes 
Webinars No 
Live Training (Online) Yes 
In Person No 

Vendor Details

Company Name

QuoData

Country

Germany

Website

www.quodata.de/content/prolab-software-interlaboratory-studies-quodata-gmbh

Vendor Details

Company Name

QiSOFT

Founded

1987

Country

United Kingdom

Website

www.qisoft.com

Product Features

Quality Management

Audit Management No 
Complaint Management No 
Compliance Management No 
Corrective and Preventive Actions (CAPA) No 
Defect Tracking No 
Document Control No 
Equipment Management No 
ISO Standards Management No 
Maintenance Management No 
Risk Management No 
Supplier Quality Control No 
Training Management No 

Product Features

Quality Management

Audit Management No 
Complaint Management Yes 
Compliance Management Yes 
Corrective and Preventive Actions (CAPA) Yes 
Defect Tracking Yes 
Document Control Yes 
Equipment Management Yes 
ISO Standards Management No 
Maintenance Management No 
Risk Management No 
Supplier Quality Control Yes 
Training Management No 

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