Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
PaKalite serves as a comprehensive quality management system tailored for small to mid-sized manufacturers in the automotive and industrial sectors, adhering to standards such as IATF 16949, ISO 9001/14001/45001, AIAG (including PPAP, APQP, MSA, SPC), and VDA 6.3.
The system comprises 17 interconnected modules, which include elements for PPAP (18 elements, PSW, MSA/GRR), phases for APQP (5 phases), various audit types (14 types, question bank, scoring, findings leading to CAPA), KPI scorecards (featuring targets, deviation alerts, and supplier ratings), as well as inspection and control plans (12 types, utilizing SPC Cp/Cpk, quarantine, and EN 10204 certifications). Additional modules facilitate calibration, drawing revision control, nonconformity management (NCR/8D), continuous improvement practices (like Kaizen and 5S), supplier quality assurance, management reviews, meeting tracking, HR competence and training, TPM maintenance, occupational health and safety, and document management.
These modules work in synergy: for instance, an audit finding can initiate a corrective action, and persistent KPI deviations can automatically trigger responses. The platform operates in the cloud and is complemented by a Windows desktop client and an Android application designed for shop-floor use. Moreover, it supports PDF reporting, Excel data importation, role-based access permissions, and ensures data isolation per company, all while offering a free plan and featuring a Turkish interface for user accessibility. This comprehensive approach enhances operational efficiency and quality assurance across diverse manufacturing processes.
Description
eDeviation provides comprehensive tools for assessing and managing Protocol Deviations. It streamlines processes from software design and validation to gathering necessary documentation and exporting information for the Trial Master File (TMF), thereby alleviating the burden on clinical teams who may face risks from improperly assessed or overlooked protocol deviations, whether they occur once or multiple times. As a component of Ethical's eClinical Software Platforms, eDeviation® enhances the efficiency and accuracy of clinical trial management. Whether evaluations are conducted by a dedicated independent committee or by your own research team, our software can be tailored to meet your specific requirements. The integration of forms, workflows, and export functions ensures adherence to GxP standards and fosters effective study management. Additionally, this platform allows study teams, investigators’ sites, and committee members to collaborate online in real-time, facilitating quicker decision-making, reaching consensus, and ensuring the prompt handling of protocol deviation assessments and management. Ultimately, eDeviation® enhances the overall integrity and efficiency of clinical trial processes, contributing to better outcomes in research.
API Access
Has API
API Access
Has API
Screenshots View All
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Integrations
No details available.
Integrations
No details available.
Pricing Details
$0
Free Trial
Free Version
Pricing Details
No price information available.
Free Trial
Free Version
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Deployment
Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Customer Support
Business Hours
Live Rep (24/7)
Online Support
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Types of Training
Training Docs
Webinars
Live Training (Online)
In Person
Vendor Details
Company Name
PaKalite
Founded
2022
Country
Turkey
Website
pakalite.com
Vendor Details
Company Name
eDeviation
Website
www.protocoldeviation.com/eDeviation-software
Product 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
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning