Quality Records (QR) Control Codes

K

klcuellar

Hello! Can anybody share his or her idea regarding quality records control codes?

We have audited and the auditor noted that our masterlist of quality records do not have QR control codes which shall be interfaced with documents, procedures, and other records for easy identification/retrieval.

I hope somebody who has an idea or sample could share asap. Thanks! :)
 
K

keres

By my opinion your auditor is right. This is not mandatory requirement but is logic and good practice.
 
K

klcuellar

By my opinion your auditor is right. This is not mandatory requirement but is logic and good practice.

thanks for the opinion. but do you have any idea on how we could address this? i thought it would be very tedious for us if we will assigned a unique code for each type of record. do you have any sample of Masterlist of Quality Records? template or format? :)
 
K

keres

thanks for the opinion. but do you have any idea on how we could address this? i thought it would be very tedious for us if we will assigned a unique code for each type of record. do you have any sample of Masterlist of Quality Records? template or format? :)

I suppose you have templates for mandatory records by your procedures. You may create rules for code identification. For example:
P001 Control of documents procedure
FM-001.001 Request for document change
...
P002 Control of records procedure
FM-002.001 Masterlist of records
...
P003 Human resourses
FM-003.001 Request for training
FM-003.002 Training protocol
In FM-002.001 Masterlist of records you can list all of your templates for the records (FM - form), not Procedures (P) with their numbers, names, revision e.t.c.
It is just a simple table.
 
Q

QAMTY

Hi Keres

Please explain, Is not mandatory the identification, 4.2.4 Control of Records?

"The organization shall establish a documented procedure to define the controls needed for the identification,storage, protection, retrieval, retention and disposition of records."

Thanks
 
K

klcuellar

I suppose you have templates for mandatory records by your procedures. You may create rules for code identification. For example:
P001 Control of documents procedure
FM-001.001 Request for document change
...
P002 Control of records procedure
FM-002.001 Masterlist of records
...
P003 Human resourses
FM-003.001 Request for training
FM-003.002 Training protocol
In FM-002.001 Masterlist of records you can list all of your templates for the records (FM - form), not Procedures (P) with their numbers, names, revision e.t.c.
It is just a simple table.

Yes actually, we do have a separate Masterlist of Forms where all our templates are indicated. and we have another Masterlist of Records where all of the filled-out forms are indicated. it is in here, in the Masterlist of Records, where our auditor is suggesting to have a different code for each record aside from the code for each forms.

Meaning a form (unaccomplished) has a form code. and once it has been accomplished and become a record, a different code shall be assign. have you encountered something like this? for example, a Document Approval Request Form has a code of FM-CSFP-QMS-01, and once accomplished, a separate code shall be assign. that is, as per the observation of the auditor.:(
 
K

keres

Hi Keres

Please explain, Is not mandatory the identification, 4.2.4 Control of Records?

"The organization shall establish a documented procedure to define the controls needed for the identification,storage, protection, retrieval, retention and disposition of records."

Thanks

I mean it is not mandatory to write masterlist of quality records and have QR control codes interfaced with documents, procedures, and other records in this masterlist.

You are right the identification is requirement. But not mandatory in masterlist of records. There are many ways to do this.
 
K

keres

Yes actually, we do have a separate Masterlist of Forms where all our templates are indicated. and we have another Masterlist of Records where all of the filled-out forms are indicated. it is in here, in the Masterlist of Records, where our auditor is suggesting to have a different code for each record aside from the code for each forms.

Meaning a form (unaccomplished) has a form code. and once it has been accomplished and become a record, a different code shall be assign. have you encountered something like this? for example, a Document Approval Request Form has a code of FM-CSFP-QMS-01, and once accomplished, a separate code shall be assign. that is, as per the observation of the auditor.:(

Did you mean a separate code for the template and another for filled-out form?
 
K

klcuellar

I mean it is not mandatory to write masterlist of quality records and have QR control codes interfaced with documents, procedures, and other records in this masterlist.

You are right the identification is requirement. But not mandatory in masterlist of records. There are many ways to do this.

Since it is not mandatory to have QR control codes in the masterlist, what other ways can we answer the observation cited by our auditor? like to address his issue on records "identification"? :(
 
Thread starter Similar threads Forum Replies Date
G Creating a "Records Policy" - Control of Quality Records Records and Data - Quality, Legal and Other Evidence 13
A Action on Quality Records - Approve, Update and Carry Out Revision Control Records and Data - Quality, Legal and Other Evidence 10
F ISO 9001:2000 Clause 4.2.4 - Control of Quality Records - What constitutes a record? Records and Data - Quality, Legal and Other Evidence 42
Claes Gefvenberg 4.16 - Procedure for control of quality records Records and Data - Quality, Legal and Other Evidence 2
I Control of Quality Records, 4.16, there is the reference to "collection" Records and Data - Quality, Legal and Other Evidence 2
R Control of Quality Records - What are the quality records required by QS-9000? Records and Data - Quality, Legal and Other Evidence 3
R Control of Quality Records - What is the required retention time? Records and Data - Quality, Legal and Other Evidence 6
G Does FDA allows remote approvals of quality documentation. Is there any specific guidance on signing any quality records remotely? Document Control Systems, Procedures, Forms and Templates 1
D Are Supplier Quality Agreements Quality Records ? Other Medical Device Regulations World-Wide 9
U Manufacturing solutions and keeping records on quality Content CE Marking (Conformité Européene) / CB Scheme 3
I Date of Quality Management System - Training Records ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 19
Q Do hard copies of quality records have to be retained? ISO 13485:2016 - Medical Device Quality Management Systems 2
R Custom Records and Quality Systems - Products that change frequently Other US Medical Device Regulations 3
B Quality Records - Should any record be signed? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
B Records Destroyed - Hurricane Harvey has likely destroyed our Quality Systems Records Records and Data - Quality, Legal and Other Evidence 10
R 21 CFR Part 820.186 - Types of Quality System Records Document Control Systems, Procedures, Forms and Templates 1
S Retention time requirement for various for quality records Records and Data - Quality, Legal and Other Evidence 1
S Atlassian and Plugins for Quality System/Records? Quality Assurance and Compliance Software Tools and Solutions 1
C Incremental revisions to Quality Manual, and Training Records Document Control Systems, Procedures, Forms and Templates 2
M Contractors with poor Quality Records ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9
K Integrating acquired existing product into Quality Management System Records ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
A Are all In-Process Quality Records required in final QA Batch Record Review. 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 9
J Quality Records Register Requirements - ISO 9001:2008 Records and Data - Quality, Legal and Other Evidence 31
H Must I mention "records kept" in the Quality Manual itself ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 11
L Storage Cabinets for Quality Documentation (Procedures and Records) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
P NQA-1 Requirement 17 Quality Records - Facility Types and Temporary Storage Various Other Specifications, Standards, and related Requirements 5
M Suggestions for Handling Quality Records ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
M What to do about missing Quality Records? Records and Data - Quality, Legal and Other Evidence 11
M Quality Records Matrix Content and Revision Records and Data - Quality, Legal and Other Evidence 6
N Quality Records - Password and Anti-virus Protection Records and Data - Quality, Legal and Other Evidence 3
H Review and Approval in Quality Records? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
P Obsolete Quality Records - Approval Prior to Disposal Records and Data - Quality, Legal and Other Evidence 15
I Do ALL Quality Records Require Approval? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
P Quality formats - ISO 13485 Design and development related records and formats ISO 13485:2016 - Medical Device Quality Management Systems 7
S Retention Periods of Quality Records Records and Data - Quality, Legal and Other Evidence 1
A Examples of Quality Records Master List ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
A Corrective Action for lost project quality records ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
A Are environmental compliance documentation quality records? Document Control Systems, Procedures, Forms and Templates 5
J ISO 9001:2000 4.2.3- Quality Records, Production Travelers Records and Data - Quality, Legal and Other Evidence 9
S Retention time of quality records for parts with Critical (safety) Characteristics? Document Control Systems, Procedures, Forms and Templates 2
C Need a procedure or outline on Good Practices for Completing Quality Records/Document Document Control Systems, Procedures, Forms and Templates 2
Q Signature on Management Review Minutes - Quality Records ISO 13485:2016 - Medical Device Quality Management Systems 5
T Sample Retention Requirements - Quality Records procedure - ISO13485 ISO 13485:2016 - Medical Device Quality Management Systems 8
T Is there a minimum retention time for any of the Quality Records? ISO9001 Records and Data - Quality, Legal and Other Evidence 8
K Records - Are weekly purchasing reports, backlog reports, etc., Quality Records? Records and Data - Quality, Legal and Other Evidence 4
R Procedure does not adequately identify quality records - Audit Minor NC - Why? General Auditing Discussions 8
H Formats for Master List of Quality Records (MQR) & Document Change Request Form (DCR) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
M Quality records kept "off site", is it ok or not? Records and Data - Quality, Legal and Other Evidence 19
Q Minimum Quality records required by ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 1
C How often will I update the quality records list? We have about 189 quality records Document Control Systems, Procedures, Forms and Templates 6

Similar threads

Top Bottom