CAPA Corrective and Preventive Action Software with Complete Visibility and Analysis

NIIX Corrective and Preventive Action software or CAPA software provides company to controls the CAPA process right from creation to validation and closure. Identifies and addresses the root causes of quality issues while supporting ISO compliance, lowering risk of business impact and repeat issues, and fostering continuous improvement to achieve QMS objective.

Making Corrective and Preventive Actions Sustainable

NIIX Corrective and Preventive Action software is available in one CAPA form. However, you can amend to either a separate Corrective Action Request or Preventive Action Request. It enables you to capture deficiencies from every aspect of your organization, identify, anticipate and correct nonconformances from root cause analysis to efficiently manage their resolution with action planning, implementation, and review and final verification.

CAPA Software that Foster ISO Standard Culture

Effective approach with CAPA initiation, investigation, root cause analysis, risk assessment planning & implement action plans, effectiveness review, resolution activities and verification.
Eliminate traditional manual work by automating CAPA processes with an intuitive web-based system. Easily collaborate with other QMS software include customer complaint, audit management, risk management, gap analysis and more.

Amendable CAPA Corrective and Preventive Action Form

Easily customize CAPA template to suit ISO standard requirement using built in intuitive drag and drop design tools.

Intuitive Analytics CAPA Report

Real-time data, analytics, and comprehensive CAPA report with historical data to identify trends, common cause, corrective action for better decision making.

Support 8D CAPA Tracking Software Methodologies

Support the eight disciplines (8D) model of problem-solving CAPA methodologies.

Due Date Alert

Set the due date for each CAPA according to your company policy. Auto notification for each task ensure no overlooked.

Multiple Supporting Document

Easily attached supporting document include image, video as a proof to the non-complaince and completion of task.

Investigate, Identify Root Cause and Risk Assessment

Investigating defects and documenting root cause and performing risk assessment along with the resolution and its effectiveness verification.

Centralized and Consistency

Record and track non-conformances and root causes at centralize cloud-based platform ensure consistency.

Integrated with Audit Report

Easily integrate with Audit Report for easy cross referring purposes.

Documented Nonconformances

Simplify the identification and documentation of defects, initiate corrective action requests and prioritize requests for corrective action.

Exceed Compliance Requirements

Facilitate compliance with corrective and preventive action requirements including ISO 9001, ISO 14001, ISO 13485 and ISO/TS 16949, etc.

NIIX-ISO-CAPA-corrective and preventive action

CAPA Software to Improve Corporate Quality System

Provide systematic CAPA approach to cultivate corporate continual improvement, solve occurred issue and prevent recurrence.

REQUEST A DEMO

BENEFIT OF NIIX CAPA CORRECTIVE AND PREVENTIVE ACTION SOFTWARE

Transform your organization CAPA on Environmental, Health & Safety and Quality management with effective validation and verification approach.

Centralize CAPA Data

Store all CAPA records in one secure and centralized cloud based system.

Realtime Alerts

Automated real time notification alert on every new or overdue tasks to prevent overlooked.

Off-Line Mode Enabled

Capable work at off-line mode anywhere anytime and upload data upon Internet available.

Effectively Prevent Problem

Cultivate effective preventive action based on details analysis insights.

Increased Productivity

Complete automated end-to-end workflow help improve effectiveness and productivity.

Improve Communications

Centralized data foster effective communication among employees in real time.

Maintain ISO Audit Ready

Complete CAPA history and records enable ISO standard audit-ready for compliance.

Real Time Visibility

Capture detailed real-time data with powerful analytics and dashboards tool.

Easy and Simplify

Simplify failure investigations, root cause analysis and CAPA action plan.

Mobile and Tablet Friendly

Access and create CAPA’s from anywhere anytime via your tablet or smart phone.

Cost Effective

Modernize CAPA system at affordable cost to efficiently achieve ISO 9001 goal.

Cultivate QMS improvement

A systematic platform to implementing effective CAPA and cultivate QMS improvement.