Nonconformance for Compliance with FDA Regulations and ISO Quality Standards
Managing nonconformance is an integral part of an organization’s continual improvement plan, and helps to ensure compliance with FDA regulations and ISO Quality Standards.
Intellect’s nonconformance application enables organizations to capture, track and maintain accurate, auditable nonconformance records through a centralized database. Intellect’s workflow helps to automate and streamline the process for identifying, evaluating, reviewing, and handling nonconforming parts, materials, and products. View any aspect of your workflow or drilldown reports for complete transparency and reporting.
Manual systems leveraging excel or other homegrown solutions are inefficient, prone to human errors, and may delay the resolution to an incident. Intellect’s nonconformance application automates and streamlines the entire process, from data collection, follow-up, escalation, and resolution of nonconformance issues. Users know what to do and when, and can review tasks or complete approvals on any device, at any time. At the same time, discover bottlenecks, send automated email notifications and reminders that drive accountability and task completion.
Managing nonconformance with manual processes and paper can be time consuming, disconnected, and costly. Intellect nonconformance makes it easy to create a custom form, automate all steps and tasks, and keep the entire process digital. The Intellect solution tracks and streamlines every step, and empowers users in the field to complete a task or provide approval using a native mobile application with offline capabilities. Intellect nonconformance helps to route information to the right person in real-time and shorten the cycle time for resolving an incident.
Give Intellect a try today and see what it can do for your business.