SBS - The Best Value in QMS software

Sample document for integrated ISO 20000 & ISO 27001

S

santosh12

#1
i am integrating iso 20000 with iso 27001. can anybody provide the sample document for the above integration?

i have identified that some of the process in both the standards are same like incident management, management review, continuous improvement, internal audit etc...
 
Elsmar Forum Sponsor
S

santosh12

#3
yeas. i am looking for how you are preparing the documents that are common in iso 20000 and iso 27001 like security incident investigation process, control of emergency changes, change management procedure etc.
 
P

prady2581

#4
Currently I have been assigned task for implementing Iso 20000 and 27001, research work started from my side. Will come back and share my experience with you all. Meantime guidance from any team member will be appreciated.
 
Thread starter Similar threads Forum Replies Date
A Sample document on design and development activities plan for a medical device Other Medical Device Regulations World-Wide 1
S Cool Minitab Document 'Sample' - Help with FULL Version location/access? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 1
L Sample pieces for customer - still document the same? Document Control Systems, Procedures, Forms and Templates 2
L Sample of Control of Document Procedure and Control of External Documents Document Control Systems, Procedures, Forms and Templates 2
S Is Master Sample a Document? - ISO 9000:2000, Clause 3.7.2 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 32
P Looking for a Closing Document Template/Sample (Project Management) Six Sigma 3
S Document Control Presentation Sample needed Document Control Systems, Procedures, Forms and Templates 4
O ISO 13485 sample document or template - Class II medical device ISO 13485:2016 - Medical Device Quality Management Systems 16
R Document that specifies PQ and sample size ISO 13485:2016 - Medical Device Quality Management Systems 1
G Sample Report to justify additional Document Control workforce Document Control Systems, Procedures, Forms and Templates 3
A Clinical assessment sample size - Medical device Class IIb implantable (93/42 directive) EU Medical Device Regulations 2
M Sample record for verification performed by importers before placing a device on the market EU Medical Device Regulations 0
P Sample Size for Distribution Simulation Testing Inspection, Prints (Drawings), Testing, Sampling and Related Topics 11
E Any sample of a full software life cycle IEC 62304 report ( any class )? IEC 62304 - Medical Device Software Life Cycle Processes 1
G Where to buy Template / sample SCSMS Manual, checklist Supply Chain Security Management Systems 1
C Stress / Challenge Conditions for Design Verification Testing to Reduce Sample Size 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 11
K How can Acceptance Number and Reject Number be larger than Sample Size on Z1.4 Table? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 8
P MSA - what exactly mean "system" and master sample Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 2
J Validation Sample Size for Tray Seal Qualification and Validation (including 21 CFR Part 11) 3
D Design Verification Sample Size vs Repeats Statistical Analysis Tools, Techniques and SPC 9
S Determining sample sizes for PQ Qualification and Validation (including 21 CFR Part 11) 4
M Minimum sample size - Guidance and statistical rationale Inspection, Prints (Drawings), Testing, Sampling and Related Topics 3
L Sample Procedure from Contract Manufacturer Prospective ISO 14971 - Medical Device Risk Management 1
D Adding a Class I to a sample box Canada Medical Device Regulations 5
P Unrealistic Packaging Validation Sample Size 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 41
M ISO 9001:2015 case study sample ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
M Sample of Nonconformity report for ISO 9001:2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
A Sample Agreement available for Outsourcing Medical Device Design activity? ISO 13485:2016 - Medical Device Quality Management Systems 1
B Control chart and sample time Statistical Analysis Tools, Techniques and SPC 1
J Control chart for huge sample size Statistical Analysis Tools, Techniques and SPC 9
D How to list multi-product sample pack in GUDID 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
S Is there a standard for sample size during R&D phase Other ISO and International Standards and European Regulations 18
M Minitab assistant: 1-Sample % Defective Test Using Minitab Software 1
J Sample size definition in an Automotive SMT pilot lot run Misc. Quality Assurance and Business Systems Related Topics 1
T ISO 27001 sample audit report IEC 27001 - Information Security Management Systems (ISMS) 0
B IATF 16949 - Is a Deviation required for sample components in a prototype build? IATF 16949 - Automotive Quality Systems Standard 13
D Sample Calibration SOP for ISO 13485 General Measurement Device and Calibration Topics 4
T Sample of 1st Article Inspection Report wanted APQP and PPAP 3
E Correct way to certify hydrostatic testing when it is not 100% (and Sample Size) Various Other Specifications, Standards, and related Requirements 6
N Design Verification & Process Validation - Statistical sample sizes Design and Development of Products and Processes 2
B Determining sample size for device sterility Inspection, Prints (Drawings), Testing, Sampling and Related Topics 3
A In which EU countries would it be okay to use sample labels for registration? EU Medical Device Regulations 0
D Determining of sample size for 'Operational Qualification' AQL - Acceptable Quality Level 5
F Bayes Success run Theorem for sample size during OQ&PQ Qualification and Validation (including 21 CFR Part 11) 4
Watchcat Identification of Test Sample in Test Reports? Design and Development of Products and Processes 22
M AQL table - I need to sample 1250pcs AQL - Acceptable Quality Level 3
K The correct way of doing a 2 Sample T test Reliability Analysis - Predictions, Testing and Standards 7
I Device modifications - Clinical sample size rationale EU Medical Device Regulations 5
M Informational How to perform a clinical evaluation of medical devices – Part 1 – Overview and sample of activities Medical Device and FDA Regulations and Standards News 0
M SOP Sample for BC/ISO22301 (Business Continuity) wanted Business Continuity & Resiliency Planning (BCRP) 4

Similar threads

Top Bottom