The Audit Module is a simple and effective tool to document and manage audit results. Schedule audits Document audit findings Convert findings into a Corrective Action (CAR) and / or Preventive Action (PAR) Report and analyze results Great for internal and external audits internal QMS audits Product audits Process audits Supplier audits Customer audits The Audit Module is contained within the Quality and Q-Med Databases: The Q-Med Database is ideal for FDA regulated industries (Medical Device, Pharmaceuticals) The Quality Database is designed for Manufacturing, Aerospace, Service and other industries.

KEY FEATURES Nonconformance Tracking Escalate a Nonconformance to a Corrective Action   Corrective Actions (CAPA) Safety, Supplier, Internal Audit CARs With Validation and Verification Approvals require electronic signatures Preventive Actions (PA) Audit management Record audit findings Manage Audit Schedules Escalate to a Corrective Action or Preventive Action Meeting management Project management Customer satisfaction surveys CFR21 part 11 compliant security, activity logs, audit trails BENEFITS Complies with requirements of ISO 13485, 21 CFR Part 820, ISO 14971 ISO 9001:2015 AS9100 ISO/TS 16949 Provides a concise, electronic record of historical events, actions, and improvement No paper to get lost Efficiently maintains quality records Internal audits Corrective Action results Preventive Action results Management review or MRB meetings Nonconformances Customer satisfaction surveys Improve product … Continue reading Q-Med Database