Grand Avenue Software
A web-based quality system software suite that helps medical device companies automate their processes and simplify regulatory compliance. Modules include: Audit Management, CAPA, Complaint Handling, Design Control, Document Control, Equipment Management, Nonconforming Materials Reporting, Supplier Management and Training Management. Designed from the beginning for ISO 13485 and 21 CFR Part 11 compliance. Audit results are recorded for each requirement in the audit. Requirements are marked as conforming, nonconforming, or not applicable. Each result may be detailed with one or more findings. Findings that may be recorded include observations, major nonconformances, and/or minor nonconformances. Findings may result in Corrective and Preventive Actions (CAPA) and/or may be documents with audit actions already completed.
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IMS Compliance Manager
Compliance Manager is a Software As A Service application that allows you to manage: Documents - Add, update, archive and manage your Policies, Procedures, Forms and Templates. Projects - Manage your projects and documentation allowing team members to share project information. Tasks - Manage tasks, audits, nonconformances, corrective & preventive actions, complaints and incidents. Alerts - Manage e-mail alerts to improve timely close out of corrective & preventive actions. Incidents - Manage incidents, investigations, resolutions and root cause analysis. Training - Manage employee records, training logs and appraisals. Suppliers - Manage supplier records and performance evaluations. Reports - Produce reports on Audit Results, Root Cause Analysis, Training, and Supplier Performance. Manage e-mail alerts to improve the timely close-out of corrective actions. Manage supplier records and performance evaluations.
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QualityPro by TecWork
QualityPro by TecWork is a modern, ๐๐ง๐ญ๐๐ซ๐ฉ๐ซ๐ข๐ฌ๐-๐ ๐ซ๐๐๐ ๐ฐ๐๐/๐๐ฅ๐จ๐ฎ๐-๐๐๐ฌ๐๐ ๐๐ฎ๐๐ฅ๐ข๐ญ๐ฒ ๐๐๐ง๐๐ ๐๐ฆ๐๐ง๐ญ ๐๐ฒ๐ฌ๐ญ๐๐ฆ (๐๐๐) designed to help manufacturing , automotive, and regulated organizations strengthen compliance, reduce operational risk, and build a proactive quality culture.
Unlike traditional systems that only store documentation, ๐๐ฎ๐๐ฅ๐ข๐ญ๐ฒ๐๐ซ๐จ ๐๐๐ ๐๐จ๐๐ญ๐ฐ๐๐ซ๐ connects quality processes into one intelligent platformโensuring clarity, accountability, and audit readiness across the entire organization.
QualityPro centralizes critical QMS workflows including:
โถ Non-Conformance & Deviation Management
โถ Corrective and Preventive Actions (CAPA)
โถ Complaint Handling & Customer Quality Events
โถ Audit Planning & Execution
โถ Calibration & Equipment Management
โถ Inspection & Quality Control
โถ Document Control
โถ Training Management & Competency Tracking
โถ Risk Management & Continuous Improvement
โถ Change Management
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ARMATURE Fabric
With ARMATURE Fabricโข you can manage your accreditation, certification, credentialing, audit, quality, and compliance activities within a single platform. Our software enables you to save time, operate more effectively and securely, and better serve your stakeholder communities.
Whether you are managing institutional, programmatic, or specialized accreditation programs; certifying individuals, products, or organizations; conducting audits or assessments; or resolving non-conformances or other issues, ARMATURE Fabric can make it easier and more efficient for you and your stakeholders.
Our secure, cloud-based software allows you to collect data in multiple ways (through online applications, audits, assessments, self-evaluations, inspections, forms, and surveys); manage your accreditation, certification, audit, and compliance workflows; capture and manage documents and artifacts, identify and remediate issues; generate reports; and spot new trends.
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