Definition Retention Zone - What exactly are you calling zones of retention?

Download Free White Paper
Elsmar Forum Sponsor
D

D.Fortin

#2
#2
Audit QS 9000

HELP............HELP...........HELP....

J'ai eu la visite de mes clients.
Durant l'audit ils m'on signalé que je DEVAIS avoir mes zones de rétention cadenassées.
Est-ce qu'il est obligatoire que les zones de rétention soient inaccessibles.......

------------------
 
D

Dan Larsen

#4
#4
Sorry I don't understand French, but I think I get the gist.

Personally, I don't like locked up nonconforming material areas. If I lock them, how can the nonconforming material freely move INTO the area? I've fought this with many customers, and I generally win.

NCM areas are defined. ANYONE can put material INTO the area. Only certain people can move material OUT. Once this is defined procedurally, it becomes a training issue.
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
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
B Document retention Policy for Japan's PMDA Japan Medical Device Regulations 1
B Document Retention Policy for NMPA China Medical Device Regulations 1
B Document Retention period for MHRA submission UK Medical Device Regulations 0
M Record Retention Verbiage Needed for "Lifetime" Retention EU Medical Device Regulations 14
H Document retention period Canada Medical Device Regulations 2
E Raw data retention for Diagnosis Results EU Medical Device Regulations 4
P Retention Samples for medical devices ISO 13485:2016 - Medical Device Quality Management Systems 2
L Retention Period for visitor's log IEC 27001 - Information Security Management Systems (ISMS) 8
Q ISO 9001/IATF 16949 Audit Finding Question - Document Retention IATF 16949 - Automotive Quality Systems Standard 11
E Record Retention - Raw Material (Steel Certs) Records and Data - Quality, Legal and Other Evidence 3
C Retention of QMS Plans and Reports ISO 13485:2016 - Medical Device Quality Management Systems 5
J Requirement for Retention of Records of Withdrawn Documents of External Origin Document Control Systems, Procedures, Forms and Templates 3
P PPAP samples retention time IATF 16949 - Automotive Quality Systems Standard 5
M Retention period of documents and records ISO 13485:2016 - Medical Device Quality Management Systems 1
B Retention Samples when Customer Leaves Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 1
D IATF16949 7.5.3.2.1 Record Retention - Our Product or Customer Product? Elsmar Cove Forum Suggestions, Complaints, Problems and Bug Reports 1
R Document Retention - Discard hard-copies after scanning? ISO 13485:2016 - Medical Device Quality Management Systems 2
M Defining and Documenting Record Retention CE Marking (Conformité Européene) / CB Scheme 5
Q AS9120B flow down to external providers: Records Retention AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
WEAVER Retention of golden samples for GR&R Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 0
N ISO 13485 Quality Record Retention Period ISO 13485:2016 - Medical Device Quality Management Systems 4
L VDA 1 Documented Information and Retention (new revision 4, August 2018) VDA Standards - Germany's Automotive Standards 0
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
L Pest Control Log Retention Time Frame ISO 13485:2016 - Medical Device Quality Management Systems 5
T MDR - Regarding the “Retention Period” of Documents and Records CE Marking (Conformité Européene) / CB Scheme 11
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
C Record retention for defunct customers? ISO 13485:2016 - Medical Device Quality Management Systems 11
A Determining Retention Period for Medical Device QMS documents Document Control Systems, Procedures, Forms and Templates 5
D Document Retention Policy IATF 16949 - Automotive Quality Systems Standard 5
B Interpretation of Customer Specific Requirements of Continental - Records Retention Customer and Company Specific Requirements 6
T Record Retention Requirements - IATF 16949 Clause 7.5.3.2.1 Records and Data - Quality, Legal and Other Evidence 15
D PMA A&P Document (i.e. Promotional Brochures, Flyers) Retention Requirements Other US Medical Device Regulations 10
J Retention Requirements of Complaint Medical Devices Customer Complaints 2
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
L GMW15920-2010 Records Retention for GM Customer and Company Specific Requirements 3
S Retention time requirement for various for quality records Records and Data - Quality, Legal and Other Evidence 1
x-files Control of Records - Retention Time vs. Retention Period Document Control Systems, Procedures, Forms and Templates 5
V Tie-wrap pull test to verify contact retention Manufacturing and Related Processes 6
P Records Retention and Disposition - ISO 9001:2008 Requirements Records and Data - Quality, Legal and Other Evidence 5
D Production Record Retention Requirements Records and Data - Quality, Legal and Other Evidence 9
V Inactive Gauge Retention Time - PPAP Section 6 Requirements APQP and PPAP 1
D Contact Retention Tools Question General Measurement Device and Calibration Topics 3
C Financial Records Retention Requirements for a Manufacturing Company Records and Data - Quality, Legal and Other Evidence 3
S Retention of Training Records question Training - Internal, External, Online and Distance Learning 2
S Are there any new FDA requirements on Record Retention ? US Food and Drug Administration (FDA) 4

Similar threads

Top Bottom