Formats for Master List of Quality Records (MQR) & Document Change Request Form (DCR)

H

harishankar77

#1
Hi All,

We are in the process of implementing QMS in my organisation. Can anyone share the formats of the Master List of Quality Records (MQR) and Document Change Request Form (DCR)??

Thanks,
Hari Shankar
 
Last edited by a moderator:
Elsmar Forum Sponsor
Q

QCAce

#2
harishankar77 said:
Hi All,

We are in the process of implementing QMS in my organisation. Can anyone share the formats of the Master List of Quality Records (MQR) and Document Change Request Form (DCR)??

Thanks,
Hari Shankar
Attached is a spreadsheet we currently use as our Master Record Retention List. It is still under development.

Our document change request form is a form in an Access database. A picture is attached.
 

Attachments

Thread starter Similar threads Forum Replies Date
T Different Formats for SOPs/Work Instructions? Document Control Systems, Procedures, Forms and Templates 5
M AS9102 FAI Report formats - Boxes in form 1, 2, 3 of AS9102 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
V Should template/formats be pre configured to claim 21 CFR part 11 compliance? Qualification and Validation (including 21 CFR Part 11) 5
T Corrective Action Reports - Alternative Formats Nonconformance and Corrective Action 1
V Qualification & Management Of Contract Quality Control Lab - Formats & Templates US Food and Drug Administration (FDA) 0
Q Control Of Documents and Forms - Formats and Numbering Document Control Systems, Procedures, Forms and Templates 3
D Good Formats to use for CAR's/CAPA's for Safety Issues or Injuries Nonconformance and Corrective Action 6
G R&D (Research and Development) & Workorder Formats Document Control Systems, Procedures, Forms and Templates 2
E MSA 3th edition vs. 4th - What are the topics, formats, criteria, new formulas, etc. Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 1
P ISO 20000 Sample Procedures and Formats IT (Information Technology) Service Management 10
Q Resume Formats - What Resume Format is Best for You? Career and Occupation Discussions 5
S MSA 4th Edition formats in Excel wanted - GR&R, Bias, Stability and Linearity Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 8
A ISO 9001 Documentation Formats - Issue date for first issue ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
A Acceptable Part Number formats in the Aerospace industry Federal Aviation Administration (FAA) Standards and Requirements 1
M TPM Formats & Implementation Methodology Lean in Manufacturing and Service Industries 1
chris1price Medical Device Labelling Regulatory Requirements - Barcode Formats ISO 13485:2016 - Medical Device Quality Management Systems 3
P Quality formats - ISO 13485 Design and development related records and formats ISO 13485:2016 - Medical Device Quality Management Systems 7
P Design Input Proposal and Design Control Checklist Formats wanted ISO 13485:2016 - Medical Device Quality Management Systems 1
J Converting solid model formats for a Calypso CMM Inspection, Prints (Drawings), Testing, Sampling and Related Topics 3
C Monthly Status Report - Monthly Reporting for each department - I need some formats ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
K QMS standard formats - Internship on implementation of QMS in a company Quality Management System (QMS) Manuals 4
Y Corrective & Preventive Action form formats Document Control Systems, Procedures, Forms and Templates 3
Marc Resumes - How to Write a Resume, Formats and Templates Career and Occupation Discussions 25
H Need advise on formats to use when writing procedures Document Control Systems, Procedures, Forms and Templates 14
T Formats for Turtle Diagram Models for a Variety of Different System Models Process Maps, Process Mapping and Turtle Diagrams 27
N Document Formats: Text Procedures vs. Flow Charts (Process Maps) Document Control Systems, Procedures, Forms and Templates 42
V Human Resources, Finance and Administration in ISO 9001 - Procedures and formats ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 60
Marc ISO 8601 - Standard for date and time formats Other ISO and International Standards and European Regulations 0
P Looking for Korean FDA Drug Master File requirements for packaging systems. Other Medical Device and Orthopedic Related Topics 1
R Device Master Record Vigilance ISO 13485:2016 - Medical Device Quality Management Systems 5
PQ Systems Getting the Most out of Master Gages Using GAGEpack Software 5
T SQL Server 2019 - Master Data Services - Validation needed? ISO 13485:2016 - Medical Device Quality Management Systems 4
R Calibrating Solid Thread Rings with HILO master General Measurement Device and Calibration Topics 1
S Master Document Register Document Control Systems, Procedures, Forms and Templates 3
B Acquired Medical Device Product Line - Documentation Requirements for Device Master Record ISO 13485:2016 - Medical Device Quality Management Systems 7
A GAGE R&R Binomial with master list (for method validation) Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 0
D Device Master Record (DMR) checklist ISO 13485:2016 - Medical Device Quality Management Systems 1
lanley liao How to understand and master the requirements of each section in API monogram product. Oil and Gas Industry Standards and Regulations 5
GreatNate Master Control QMS software Quality Tools, Improvement and Analysis 1
E Procedure ( SOP) for Device Master Record ( DMR ) and for Device History Record (DHR)? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 9
M Old Master Schedules - How Long to Keep? Document Control Systems, Procedures, Forms and Templates 4
N Master Samples - What should we be keeping? IATF 16949 - Automotive Quality Systems Standard 9
P MSA - what exactly mean "system" and master sample Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 2
G Calibration of "Master Parts" Used as Gauges Calibration Frequency (Interval) 5
I Master Document Access - ISO 9001:2015 clause 7.5.3 Document Control Systems, Procedures, Forms and Templates 5
Q Forms Master List versus Record Matrix ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
E Part 11 Compliance, Excel living documents (i.e. document master list, equipment list, approved supplier list) Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 3
R No design history file or device master record ISO 13485:2016 - Medical Device Quality Management Systems 5
Sam Lazzara Medical Device File (MDF per 13485:2016 4.2.3) versus FDA Device Master Record (DMR) ISO 13485:2016 - Medical Device Quality Management Systems 3
D Virtual Documentation via Master Flow Chart? Process Maps, Process Mapping and Turtle Diagrams 4

Similar threads

Top Bottom