MR-REC
Management Review Record Inputs, decisions, and action items from a QMS management review meeting
Retention: 10 years
Your role cannot create this record type
TR-REC
Training Record Individual or group training completion record with competency assessment
Retention: 10 years post-termination
Your role cannot create this record type
AUD-REC
Internal Audit Record Internal audit report including scope, findings, and corrective action plan
Retention: 10 years
Your role cannot create this record type
CAPA-REC
CAPA Record Corrective and preventive action record linked to CAPA subsystem
Retention: 10 years
Your role cannot create this record type
SUP-EVAL
Supplier Evaluation Record Supplier qualification evaluation and re-evaluation record
Retention: 10 years post-relationship
Your role cannot create this record type
TEST-RES
Test Result Record IQ, OQ, or PQ test execution results linked to validation protocols
Retention: 10 years
Your role cannot create this record type
DR-MIN
Design Review Minutes Formal design review meeting minutes with decisions and action items
Retention: Product lifetime + 2 years
Your role cannot create this record type
CLIN-REC
Clinical Validation Record Clinical validation study execution record and results
Retention: 15 years
Your role cannot create this record type
VIG-REC
Vigilance / PMS Record Post-market surveillance and vigilance event record
Retention: 15 years
Your role cannot create this record type
CHG-REQ
Change Request Record Documented record of a change request and its disposition
Retention: 10 years
Your role cannot create this record type
DEV-REP
Deviation / NCR Record Nonconformity or deviation report with root cause and disposition
Retention: 10 years
Your role cannot create this record type
BATCH
Batch Production Record Production batch record documenting software release components and verification
Retention: 10 years
Your role cannot create this record type