Quality Procedures, Process Instructions, Forms, and Tools Forms and Tools QSF # (if applicable) Form Name QSF-14-2 CAR PAR Directory QSF-11-1 Calibrated Equipment List QSF-14-3 Containment Plan QSF-5-4 Controlled Document Approvals QSF-5-1 Controlled Documentation Distribution Log QSF-5-3 Controlled Documentation Revision Status Log QSF-14-1 Corrective Preventative Action Report QSF-14-6 Incident Intake Sheet QSF-14-8 Incident Report QSF-14-9 Incident Report Directory QSF-17-1 Internal Audit Report QSF-17-2 Internal Audit Report Directory N/A Internal Audit Schedule QSF-6-2 Key Supplier List QSF-13-1 Lesson(s) Learned Log QSF-1-1 Management Review Meeting Summary N/A On-Call CPI Training Record QSF-14-4 Quality Investigation Notes QSF-5-2 Quality System Documentation Review QSF-14-7 Safety Check Huddle Meeting Checklist QSF-6-1 Service Provider or Supplier Evaluation QSF-14-5 Stakeholder Follow-up Form QSF-6-3 Supplier Qualification Assessment QSF-6-4 Supplier Qualification Assessment – Consultant Services Quality Assurance Procedures QSP # Name QM-Intro Quality Manual QSP-1-1 Management Responsibility QSP-1-2 Management Review Procedure QSP-2-1 Quality System Framework QSP-3-1 Service Level Agreements QSP-5-1 Document and Data Control QSP-6-1 Clinical Supplier Selection and Evaluation QSP-11-1 Control of Inspection, Measurement, and Testing Equipment QSP-13-1 Nonconformance QSP-14-1 Corrective and Preventative Action QSP-16-1 Quality Records QSP-17-1 Internal Auditing Quality Assurance Process Instructions QPI # Name QPI-5-1 Business System Data Control QPI-6-1 Product Recall QPI-9-1 iTransplant Change Request QPI-14-1 Critical Incident QPI-14-2 Complaint QPI-14-3 Incident QPI-14-4 Ornge Transportation Incident QPI-17-1 External Laboratory and Organ Recovery Audit QPI-17-2 Supplier Audit
