Record retention for defunct customers?

Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
K Record Retention For Manufacture of components ISO 13485:2016 - Medical Device Quality Management Systems 3
C Bulk Record Retention Review Records and Data - Quality, Legal and Other Evidence 4
E PMS record retention time for legacy devices EU Medical Device Regulations 1
M Record Retention Verbiage Needed for "Lifetime" Retention EU Medical Device Regulations 14
E Record Retention - Raw Material (Steel Certs) Records and Data - Quality, Legal and Other Evidence 3
D IATF16949 7.5.3.2.1 Record Retention - Our Product or Customer Product? Elsmar Cove Forum Suggestions, Complaints, Problems and Bug Reports 1
M Defining and Documenting Record Retention CE Marking (Conformité Européene) / CB Scheme 5
N ISO 13485 Quality Record Retention Period ISO 13485:2016 - Medical Device Quality Management Systems 4
Gman2 Quality Record Retention (Internal Audits, CA's) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
S Mobile app data privacy - Length of record retention in a software app Medical Information Technology, Medical Software and Health Informatics 1
S Record Retention - How long must a company keep the following records? Records and Data - Quality, Legal and Other Evidence 17
K Our local sterilizer is closing - Record Retention Question 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
T Record Retention Requirements - IATF 16949 Clause 7.5.3.2.1 Records and Data - Quality, Legal and Other Evidence 15
Pmarszal FDA Global UDI Database: Record Submission Retention Other US Medical Device Regulations 1
WCHorn Flowdown of Aerospace record retention requirements (AS9100) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
D Production Record Retention Requirements Records and Data - Quality, Legal and Other Evidence 9
S Are there any new FDA requirements on Record Retention ? US Food and Drug Administration (FDA) 4
S Aerospace Record Retention Requirements Records and Data - Quality, Legal and Other Evidence 5
D Question... Record retention Prior to FDA NDA application and approval Records and Data - Quality, Legal and Other Evidence 3
C Record retention/retrieval for 30+ years? (The lifespan of the medical device) ISO 13485:2016 - Medical Device Quality Management Systems 5
N Notification Sample Regarding Record Retention ISO 13485:2016 - Medical Device Quality Management Systems 5
M Record Retention requirements for Safety Items Document Control Systems, Procedures, Forms and Templates 7
S Electronic Record Retention per FDA Requirements - Electronic Data Capture (EDC) Records and Data - Quality, Legal and Other Evidence 4
K 820.180(b) Record Retention - Does it apply here? We act as the initial Importer 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
B 21 CFR 820.180 Quality Record Retention Requirements Document Control Systems, Procedures, Forms and Templates 1
W Calibration Record Retention Requirements Document Control Systems, Procedures, Forms and Templates 18
T Control of Records - API Q1 8th Edition Record Retention Requirements Oil and Gas Industry Standards and Regulations 7
A Canada Importer Record Retention Requirements - Disagreement with NB auditor Canada Medical Device Regulations 5
R Record Retention Requirements per FDA 820 Regulations Records and Data - Quality, Legal and Other Evidence 10
D MDD (Medical Device Directive) 6.1 Record Retention Requirements question Records and Data - Quality, Legal and Other Evidence 2
Q US Distributor Record Retention Requirements 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
P Record Retention requirements of Calibration and Verification Service Providers ISO 13485:2016 - Medical Device Quality Management Systems 11
E Approval Signature Record Retention Document Control Systems, Procedures, Forms and Templates 2
C Record Retention Time for Sterile Products 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
Q Customer Purchase Order: TS 16949 Record Retention Requirements Records and Data - Quality, Legal and Other Evidence 4
S Minimum Record Retention Period for ISO 14001 Records and Data - Quality, Legal and Other Evidence 2
S Record Retention Log - What Records are required in a Record Retention Log Records and Data - Quality, Legal and Other Evidence 7
C What is the Minimum Regulatory Requirement for Record Retention of DHR by Suppliers Records and Data - Quality, Legal and Other Evidence 9
B Training Record Retention Training - Internal, External, Online and Distance Learning 6
D Record Retention Requirements - TS 16949 Records and Data - Quality, Legal and Other Evidence 4
M Information Technology Record Retention time best practices Quality Management System (QMS) Manuals 2
Douglas E. Purdy Control of Disposition of Records - Record Retention - TS 16949 Clause 4.2.4.1 Records and Data - Quality, Legal and Other Evidence 8
T 21 CFR Part 11, "enforcement discretion" - Validation, Audit Trail, Record Retention Qualification and Validation (including 21 CFR Part 11) 4
Y Record Retention by R&D Shop After Handover ISO 13485:2016 - Medical Device Quality Management Systems 5
P ANSI NCSL Z540.1 Calibration Record Retention Period General Measurement Device and Calibration Topics 3
M Medical and Administration department Document and Record Retention policy Document Control Systems, Procedures, Forms and Templates 8
H Record Retention Time of Part Life + 1 Year Records and Data - Quality, Legal and Other Evidence 7
CarolX Record retention ideas for a sheet metal job shop supplying to a medical device mfg. ISO 13485:2016 - Medical Device Quality Management Systems 11
B Minimum retention or the date of destruction of a record - ISO 9001-2000 Para. 4.2.4 Records and Data - Quality, Legal and Other Evidence 13
J Record Control - Who are the Record Custodian and Retention Times - ISO9001 - 7.5.3 Records and Data - Quality, Legal and Other Evidence 9

Similar threads

Top Bottom