SlideShare a Scribd company logo
LIFE CYCLE MANAGEMENT OF
COMPUTERIZED SYSTEM
RAKTIM DEY
DY. MANAGER-VALIDATION AND QUALIFICATION
GRANULES INDIA LIMITED
OVERVIEW
Life cycle management of Computerized system consists of the following major steps:
• Requirements
• Development
• Validation
• Implementation/Deployment
• Control
• Maintenance and
• Retirement
COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART
Change Control
Initiation
Initial Risk Assessment
System Information
Business Requirement
GXP Relevance
ER/ES Relevance
GAMP Categorization
New System or Existing
System or Laboratory
software or Production
Equipment related or Other
control system or etc.
User Requirement
Specification (URS)
• Purpose of the system
• Brief description of the system
• Design and Environment
• Regulatory requirements
• Service Requirement
• References
1
2
3
COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART
Vendor Identification
and Assessment
Identification of Suitable vendor
Vendor assessment through audits as applicable
Finalization of the vendor
Vendor documents DS/FS/CS/operation manual Assessment
Validation Plan
Validation plan explains about how the necessary requirements will be fulfilled.
It will provide the list of life cycle documentation, role and responsibility and
define testing strategy, criteria for final acceptance, release of system and
maintenance of lifetime compliance.
Validation of computerized system shall be performed in a logical, systematic
manner and risk based approach shall be followed.
4
5
COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART
System Installation
Qualification
Type of Environment – Validation Server or Production Server
System Details like Software name, Version,
Installation Checklist (Installation of Instrument/Equipment,
Installation and Configuration of Application Software
Verification of Pre-Installation Checklist (PO, Intactness of system
components, etc.)
Deviation record, if any.
6
COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART
System Installation
Qualification
Type of Environment – Validation Server or Production Server
System Details like Software name, Version,
Installation Checklist (Installation of Instrument/Equipment,
Installation and Configuration of Application Software
Verification of Pre-Installation Checklist (PO, Intactness of system
components, etc.)
Deviation record, if any.
Summary and conclusion
7
COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART
System Operation
Qualification
Roles of different personnel involved in the qualification of system
Reference documents to perform OQ
Test Planning [Test Items, Components and functions to be tested]
Test Strategy [Test Objective, Test Approach, Recording of results,
Acceptance criteria]
Deviation record, if any
Summary and conclusion
8
COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART
System Performance
Qualification
Roles of different personnel involved in the qualification of system
Reference documents to perform PQ
Test Planning [Test Items, Components and functions to be tested]
Test Strategy [Test Objective, Test Approach, Recording of results,
Acceptance criteria]
Deviation record, if any
Summary and conclusion
9
COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART
Validation
Summary Report
Objective: The objectives of this VSR are to summarize the results
of the validation effort for <Computerized system> to show that
the system is validated according to standards and applicable
regulatory requirements.
Deviations from the Validation Plan, if any
Follow up actions w.r.t the deviations
Summary and Assessment of System Life Cycle Documentation,
e.g. Name Document ID
User requirement Specification To record
Initial Risk Assessment To record
Validation Plan To record
Function Specification To record
Traceability Matrix To record
Risk Assessment (FMECA) To record
Post Implementation review, System acceptance and release
10
COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART
Traceability
Matrix
URS ID
URS specification or
Parameter
IQ test ID OQ test ID PQ test ID
Remarks
If any
URS-01
URS-02
URS-03
URS-04
Traceability matrix outline the User Requirement and the section in which
that particular requirement is tested.
11
COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART
Post
Implementation
Review
Validation Documents Review
Deviation/Change Record Review
Audit Trail Record Review
System Security and Access Control Review
Software and Data Backups Review
Training Record Review
SOPs Review
12
COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART
Periodic Review
Sr.
No.
Name of Computerized
System
Version no.
/Release no.
Frequency of
Review
Date of
Validation
Last Periodic
Review done
on
Next Periodic
Review due
on
Periodic
Review
done on
Periodic
Review
Report No.
Periodic Review of system shall be conducted every year, to assess the continuity of
system operation. Any upgradation/Change in the system shall be assessed for re-
qualification
13
COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART
Revalidation Any major Changes/ Upgradation in the system needs to be re-validated.
System
Retirement
Any system which has gone outdated /Non-Functional needs to be obsoleted through
proper documentation. A risk assessment may be performed to assess the impact on
the particular system retirement on Product/Business continuity/Output etc.
14
15
THANK YOU

More Related Content

What's hot

Computer system validation
Computer system validation Computer system validation
Computer system validation
ShameerAbid
 
Prior Approval Supplements (PAS)
Prior Approval Supplements (PAS)Prior Approval Supplements (PAS)
Prior Approval Supplements (PAS)
Nirma University
 
Change control
Change controlChange control
Change control
ratan mukhopadhyay
 
Overview on “Computer System Validation” CSV
Overview on  “Computer System Validation” CSVOverview on  “Computer System Validation” CSV
Overview on “Computer System Validation” CSV
Anil Sharma
 
Gamp Riskbased Approch To Validation
Gamp Riskbased Approch To ValidationGamp Riskbased Approch To Validation
Gamp Riskbased Approch To Validation
Rajendra Sadare
 
Risk assessment for computer system validation
Risk assessment for computer system validationRisk assessment for computer system validation
Risk assessment for computer system validation
Bangaluru
 
Computer System Validation - The Validation Master Plan
Computer System Validation - The Validation Master PlanComputer System Validation - The Validation Master Plan
Computer System Validation - The Validation Master Plan
Wolfgang Kuchinke
 
Computer System Validation
Computer System ValidationComputer System Validation
Computer System Validation
chitralekha48
 
21 CFR Part 11 checklist software.pptx
21 CFR Part 11 checklist software.pptx21 CFR Part 11 checklist software.pptx
21 CFR Part 11 checklist software.pptx
AartiVats5
 
Implementing the TMF Reference Model
Implementing the TMF Reference ModelImplementing the TMF Reference Model
Implementing the TMF Reference Model
Montrium
 
FDA Inspections are Different from ISO Audits, So Don't Treat Them the Same -...
FDA Inspections are Different from ISO Audits, So Don't Treat Them the Same -...FDA Inspections are Different from ISO Audits, So Don't Treat Them the Same -...
FDA Inspections are Different from ISO Audits, So Don't Treat Them the Same -...
April Bright
 
computer system validation
computer system validationcomputer system validation
computer system validation
Gopal Patel
 
ASQ CQA Part 1: Auditing Fundamentals
ASQ CQA Part 1: Auditing FundamentalsASQ CQA Part 1: Auditing Fundamentals
ASQ CQA Part 1: Auditing Fundamentals
Seetharam Kandarpa ASQ CMQ/OE, CPGP, CQA
 
Product lifecycle management
Product lifecycle managementProduct lifecycle management
Product lifecycle management
garimasaini33
 
eTMF in the fast lane
eTMF in the fast laneeTMF in the fast lane
eTMF in the fast lane
dirkbeth
 
Computer System Validation Training
Computer System Validation TrainingComputer System Validation Training
Computer System Validation Training
NetZealous LLC
 
Process Validation for Beginners - FDA - EMA Approach
Process Validation for Beginners - FDA - EMA ApproachProcess Validation for Beginners - FDA - EMA Approach
Process Validation for Beginners - FDA - EMA Approach
GMP EDUCATION : Not for Profit Organization
 
ANDA Submission.pptx
ANDA Submission.pptxANDA Submission.pptx
ANDA Submission.pptx
KuntalKapure
 
Computer systems compliance
Computer systems complianceComputer systems compliance
Computer systems compliance
Muhammad Luqman Ikram
 
Gamp 5 overview by jaya prakash ra
Gamp 5 overview by jaya prakash raGamp 5 overview by jaya prakash ra
Gamp 5 overview by jaya prakash ra
JAYA PRAKASH VELUCHURI
 

What's hot (20)

Computer system validation
Computer system validation Computer system validation
Computer system validation
 
Prior Approval Supplements (PAS)
Prior Approval Supplements (PAS)Prior Approval Supplements (PAS)
Prior Approval Supplements (PAS)
 
Change control
Change controlChange control
Change control
 
Overview on “Computer System Validation” CSV
Overview on  “Computer System Validation” CSVOverview on  “Computer System Validation” CSV
Overview on “Computer System Validation” CSV
 
Gamp Riskbased Approch To Validation
Gamp Riskbased Approch To ValidationGamp Riskbased Approch To Validation
Gamp Riskbased Approch To Validation
 
Risk assessment for computer system validation
Risk assessment for computer system validationRisk assessment for computer system validation
Risk assessment for computer system validation
 
Computer System Validation - The Validation Master Plan
Computer System Validation - The Validation Master PlanComputer System Validation - The Validation Master Plan
Computer System Validation - The Validation Master Plan
 
Computer System Validation
Computer System ValidationComputer System Validation
Computer System Validation
 
21 CFR Part 11 checklist software.pptx
21 CFR Part 11 checklist software.pptx21 CFR Part 11 checklist software.pptx
21 CFR Part 11 checklist software.pptx
 
Implementing the TMF Reference Model
Implementing the TMF Reference ModelImplementing the TMF Reference Model
Implementing the TMF Reference Model
 
FDA Inspections are Different from ISO Audits, So Don't Treat Them the Same -...
FDA Inspections are Different from ISO Audits, So Don't Treat Them the Same -...FDA Inspections are Different from ISO Audits, So Don't Treat Them the Same -...
FDA Inspections are Different from ISO Audits, So Don't Treat Them the Same -...
 
computer system validation
computer system validationcomputer system validation
computer system validation
 
ASQ CQA Part 1: Auditing Fundamentals
ASQ CQA Part 1: Auditing FundamentalsASQ CQA Part 1: Auditing Fundamentals
ASQ CQA Part 1: Auditing Fundamentals
 
Product lifecycle management
Product lifecycle managementProduct lifecycle management
Product lifecycle management
 
eTMF in the fast lane
eTMF in the fast laneeTMF in the fast lane
eTMF in the fast lane
 
Computer System Validation Training
Computer System Validation TrainingComputer System Validation Training
Computer System Validation Training
 
Process Validation for Beginners - FDA - EMA Approach
Process Validation for Beginners - FDA - EMA ApproachProcess Validation for Beginners - FDA - EMA Approach
Process Validation for Beginners - FDA - EMA Approach
 
ANDA Submission.pptx
ANDA Submission.pptxANDA Submission.pptx
ANDA Submission.pptx
 
Computer systems compliance
Computer systems complianceComputer systems compliance
Computer systems compliance
 
Gamp 5 overview by jaya prakash ra
Gamp 5 overview by jaya prakash raGamp 5 overview by jaya prakash ra
Gamp 5 overview by jaya prakash ra
 

Similar to Life Cycle Management of Computerized System.pdf

Equipment Qualification.pptx
Equipment Qualification.pptxEquipment Qualification.pptx
Equipment Qualification.pptx
Neeraj Kumar Rai
 
Data Integrity II - Chromatography data system (CDS) in Pharma
Data Integrity II - Chromatography data system (CDS) in PharmaData Integrity II - Chromatography data system (CDS) in Pharma
Data Integrity II - Chromatography data system (CDS) in Pharma
Sathish Vemula
 
Vaidation ppt.pptx
Vaidation ppt.pptxVaidation ppt.pptx
Vaidation ppt.pptx
Aryansharma592895
 
Concept of URS,DQ,IQ,OQ,PQ
Concept of URS,DQ,IQ,OQ,PQConcept of URS,DQ,IQ,OQ,PQ
Concept of URS,DQ,IQ,OQ,PQ
dhavalrock24
 
Testing Process
Testing ProcessTesting Process
Testing Process
maheshpadwal
 
CONCEPT OF URS, DQ, IQ, OQ, PQ
CONCEPT OF URS, DQ, IQ, OQ, PQCONCEPT OF URS, DQ, IQ, OQ, PQ
CONCEPT OF URS, DQ, IQ, OQ, PQ
ROHIT
 
Webinar: How to Ace Your SaaS-based EDC System Validation for Sponsors and CROs
Webinar: How to Ace Your SaaS-based EDC System Validation for Sponsors and CROsWebinar: How to Ace Your SaaS-based EDC System Validation for Sponsors and CROs
Webinar: How to Ace Your SaaS-based EDC System Validation for Sponsors and CROs
Statistics & Data Corporation
 
Computerized System Validation.vinay (1).pptx
Computerized  System  Validation.vinay (1).pptxComputerized  System  Validation.vinay (1).pptx
Computerized System Validation.vinay (1).pptx
KIET GROUP OF INSITITUTE
 
1 - Introduction to Computerized Systems Validation - for review.pptx
1 - Introduction to Computerized Systems Validation - for review.pptx1 - Introduction to Computerized Systems Validation - for review.pptx
1 - Introduction to Computerized Systems Validation - for review.pptx
patemalabanan
 
Cleanroom Qualification
Cleanroom QualificationCleanroom Qualification
Cleanroom Qualification
Anwar Munjewar
 
Validation : Project Management
Validation : Project ManagementValidation : Project Management
Validation : Project Management
Dipen Shroff
 
Facility Qualification & Consideration of Validation Aspects
Facility Qualification & Consideration of Validation Aspects Facility Qualification & Consideration of Validation Aspects
Facility Qualification & Consideration of Validation Aspects
Apoorva Bauskar
 
Software audiit information management
Software audiit   information managementSoftware audiit   information management
Software audiit information management
Hallmark B-school
 
Computerized system validation (CSV) as a requirement for good manufacturing ...
Computerized system validation (CSV) as a requirement for good manufacturing ...Computerized system validation (CSV) as a requirement for good manufacturing ...
Computerized system validation (CSV) as a requirement for good manufacturing ...
Ahmed Hasham
 
Principle of Validation and Qualification
Principle of Validation and QualificationPrinciple of Validation and Qualification
Principle of Validation and Qualification
Pharmaguideline
 
Equipment Qualification
Equipment QualificationEquipment Qualification
Equipment Qualification
Priyanka Kandhare
 
Process and Regulated Processes Software Validation Elements
Process and Regulated Processes Software Validation ElementsProcess and Regulated Processes Software Validation Elements
Process and Regulated Processes Software Validation Elements
Arta Doci
 
Validation Program Design
Validation Program DesignValidation Program Design
Validation Program Design
bwbslide
 
Urs,dq, iq,oq,pq
Urs,dq, iq,oq,pqUrs,dq, iq,oq,pq
Urs,dq, iq,oq,pq
Māľāý Păųļ
 
Analytical instrument qualification
Analytical instrument qualificationAnalytical instrument qualification
Analytical instrument qualification
manusb07
 

Similar to Life Cycle Management of Computerized System.pdf (20)

Equipment Qualification.pptx
Equipment Qualification.pptxEquipment Qualification.pptx
Equipment Qualification.pptx
 
Data Integrity II - Chromatography data system (CDS) in Pharma
Data Integrity II - Chromatography data system (CDS) in PharmaData Integrity II - Chromatography data system (CDS) in Pharma
Data Integrity II - Chromatography data system (CDS) in Pharma
 
Vaidation ppt.pptx
Vaidation ppt.pptxVaidation ppt.pptx
Vaidation ppt.pptx
 
Concept of URS,DQ,IQ,OQ,PQ
Concept of URS,DQ,IQ,OQ,PQConcept of URS,DQ,IQ,OQ,PQ
Concept of URS,DQ,IQ,OQ,PQ
 
Testing Process
Testing ProcessTesting Process
Testing Process
 
CONCEPT OF URS, DQ, IQ, OQ, PQ
CONCEPT OF URS, DQ, IQ, OQ, PQCONCEPT OF URS, DQ, IQ, OQ, PQ
CONCEPT OF URS, DQ, IQ, OQ, PQ
 
Webinar: How to Ace Your SaaS-based EDC System Validation for Sponsors and CROs
Webinar: How to Ace Your SaaS-based EDC System Validation for Sponsors and CROsWebinar: How to Ace Your SaaS-based EDC System Validation for Sponsors and CROs
Webinar: How to Ace Your SaaS-based EDC System Validation for Sponsors and CROs
 
Computerized System Validation.vinay (1).pptx
Computerized  System  Validation.vinay (1).pptxComputerized  System  Validation.vinay (1).pptx
Computerized System Validation.vinay (1).pptx
 
1 - Introduction to Computerized Systems Validation - for review.pptx
1 - Introduction to Computerized Systems Validation - for review.pptx1 - Introduction to Computerized Systems Validation - for review.pptx
1 - Introduction to Computerized Systems Validation - for review.pptx
 
Cleanroom Qualification
Cleanroom QualificationCleanroom Qualification
Cleanroom Qualification
 
Validation : Project Management
Validation : Project ManagementValidation : Project Management
Validation : Project Management
 
Facility Qualification & Consideration of Validation Aspects
Facility Qualification & Consideration of Validation Aspects Facility Qualification & Consideration of Validation Aspects
Facility Qualification & Consideration of Validation Aspects
 
Software audiit information management
Software audiit   information managementSoftware audiit   information management
Software audiit information management
 
Computerized system validation (CSV) as a requirement for good manufacturing ...
Computerized system validation (CSV) as a requirement for good manufacturing ...Computerized system validation (CSV) as a requirement for good manufacturing ...
Computerized system validation (CSV) as a requirement for good manufacturing ...
 
Principle of Validation and Qualification
Principle of Validation and QualificationPrinciple of Validation and Qualification
Principle of Validation and Qualification
 
Equipment Qualification
Equipment QualificationEquipment Qualification
Equipment Qualification
 
Process and Regulated Processes Software Validation Elements
Process and Regulated Processes Software Validation ElementsProcess and Regulated Processes Software Validation Elements
Process and Regulated Processes Software Validation Elements
 
Validation Program Design
Validation Program DesignValidation Program Design
Validation Program Design
 
Urs,dq, iq,oq,pq
Urs,dq, iq,oq,pqUrs,dq, iq,oq,pq
Urs,dq, iq,oq,pq
 
Analytical instrument qualification
Analytical instrument qualificationAnalytical instrument qualification
Analytical instrument qualification
 

Recently uploaded

Pharmaceutics Pharmaceuticals best of brub
Pharmaceutics Pharmaceuticals best of brubPharmaceutics Pharmaceuticals best of brub
Pharmaceutics Pharmaceuticals best of brub
danielkiash986
 
REASIGNACION 2024 UGEL CHUPACA 2024 UGEL CHUPACA.pdf
REASIGNACION 2024 UGEL CHUPACA 2024 UGEL CHUPACA.pdfREASIGNACION 2024 UGEL CHUPACA 2024 UGEL CHUPACA.pdf
REASIGNACION 2024 UGEL CHUPACA 2024 UGEL CHUPACA.pdf
giancarloi8888
 
مصحف القراءات العشر أعد أحرف الخلاف سمير بسيوني.pdf
مصحف القراءات العشر   أعد أحرف الخلاف سمير بسيوني.pdfمصحف القراءات العشر   أعد أحرف الخلاف سمير بسيوني.pdf
مصحف القراءات العشر أعد أحرف الخلاف سمير بسيوني.pdf
سمير بسيوني
 
Nutrition Inc FY 2024, 4 - Hour Training
Nutrition Inc FY 2024, 4 - Hour TrainingNutrition Inc FY 2024, 4 - Hour Training
Nutrition Inc FY 2024, 4 - Hour Training
melliereed
 
Electric Fetus - Record Store Scavenger Hunt
Electric Fetus - Record Store Scavenger HuntElectric Fetus - Record Store Scavenger Hunt
Electric Fetus - Record Store Scavenger Hunt
RamseyBerglund
 
Elevate Your Nonprofit's Online Presence_ A Guide to Effective SEO Strategies...
Elevate Your Nonprofit's Online Presence_ A Guide to Effective SEO Strategies...Elevate Your Nonprofit's Online Presence_ A Guide to Effective SEO Strategies...
Elevate Your Nonprofit's Online Presence_ A Guide to Effective SEO Strategies...
TechSoup
 
skeleton System.pdf (skeleton system wow)
skeleton System.pdf (skeleton system wow)skeleton System.pdf (skeleton system wow)
skeleton System.pdf (skeleton system wow)
Mohammad Al-Dhahabi
 
MDP on air pollution of class 8 year 2024-2025
MDP on air pollution of class 8 year 2024-2025MDP on air pollution of class 8 year 2024-2025
MDP on air pollution of class 8 year 2024-2025
khuleseema60
 
How Barcodes Can Be Leveraged Within Odoo 17
How Barcodes Can Be Leveraged Within Odoo 17How Barcodes Can Be Leveraged Within Odoo 17
How Barcodes Can Be Leveraged Within Odoo 17
Celine George
 
BÀI TẬP BỔ TRỢ TIẾNG ANH LỚP 9 CẢ NĂM - GLOBAL SUCCESS - NĂM HỌC 2024-2025 - ...
BÀI TẬP BỔ TRỢ TIẾNG ANH LỚP 9 CẢ NĂM - GLOBAL SUCCESS - NĂM HỌC 2024-2025 - ...BÀI TẬP BỔ TRỢ TIẾNG ANH LỚP 9 CẢ NĂM - GLOBAL SUCCESS - NĂM HỌC 2024-2025 - ...
BÀI TẬP BỔ TRỢ TIẾNG ANH LỚP 9 CẢ NĂM - GLOBAL SUCCESS - NĂM HỌC 2024-2025 - ...
Nguyen Thanh Tu Collection
 
The basics of sentences session 7pptx.pptx
The basics of sentences session 7pptx.pptxThe basics of sentences session 7pptx.pptx
The basics of sentences session 7pptx.pptx
heathfieldcps1
 
NEWSPAPERS - QUESTION 1 - REVISION POWERPOINT.pptx
NEWSPAPERS - QUESTION 1 - REVISION POWERPOINT.pptxNEWSPAPERS - QUESTION 1 - REVISION POWERPOINT.pptx
NEWSPAPERS - QUESTION 1 - REVISION POWERPOINT.pptx
iammrhaywood
 
RESULTS OF THE EVALUATION QUESTIONNAIRE.pptx
RESULTS OF THE EVALUATION QUESTIONNAIRE.pptxRESULTS OF THE EVALUATION QUESTIONNAIRE.pptx
RESULTS OF THE EVALUATION QUESTIONNAIRE.pptx
zuzanka
 
Bonku-Babus-Friend by Sathyajith Ray (9)
Bonku-Babus-Friend by Sathyajith Ray  (9)Bonku-Babus-Friend by Sathyajith Ray  (9)
Bonku-Babus-Friend by Sathyajith Ray (9)
nitinpv4ai
 
Mule event processing models | MuleSoft Mysore Meetup #47
Mule event processing models | MuleSoft Mysore Meetup #47Mule event processing models | MuleSoft Mysore Meetup #47
Mule event processing models | MuleSoft Mysore Meetup #47
MysoreMuleSoftMeetup
 
CIS 4200-02 Group 1 Final Project Report (1).pdf
CIS 4200-02 Group 1 Final Project Report (1).pdfCIS 4200-02 Group 1 Final Project Report (1).pdf
CIS 4200-02 Group 1 Final Project Report (1).pdf
blueshagoo1
 
Beyond Degrees - Empowering the Workforce in the Context of Skills-First.pptx
Beyond Degrees - Empowering the Workforce in the Context of Skills-First.pptxBeyond Degrees - Empowering the Workforce in the Context of Skills-First.pptx
Beyond Degrees - Empowering the Workforce in the Context of Skills-First.pptx
EduSkills OECD
 
How to Predict Vendor Bill Product in Odoo 17
How to Predict Vendor Bill Product in Odoo 17How to Predict Vendor Bill Product in Odoo 17
How to Predict Vendor Bill Product in Odoo 17
Celine George
 
Educational Technology in the Health Sciences
Educational Technology in the Health SciencesEducational Technology in the Health Sciences
Educational Technology in the Health Sciences
Iris Thiele Isip-Tan
 
Geography as a Discipline Chapter 1 __ Class 11 Geography NCERT _ Class Notes...
Geography as a Discipline Chapter 1 __ Class 11 Geography NCERT _ Class Notes...Geography as a Discipline Chapter 1 __ Class 11 Geography NCERT _ Class Notes...
Geography as a Discipline Chapter 1 __ Class 11 Geography NCERT _ Class Notes...
ImMuslim
 

Recently uploaded (20)

Pharmaceutics Pharmaceuticals best of brub
Pharmaceutics Pharmaceuticals best of brubPharmaceutics Pharmaceuticals best of brub
Pharmaceutics Pharmaceuticals best of brub
 
REASIGNACION 2024 UGEL CHUPACA 2024 UGEL CHUPACA.pdf
REASIGNACION 2024 UGEL CHUPACA 2024 UGEL CHUPACA.pdfREASIGNACION 2024 UGEL CHUPACA 2024 UGEL CHUPACA.pdf
REASIGNACION 2024 UGEL CHUPACA 2024 UGEL CHUPACA.pdf
 
مصحف القراءات العشر أعد أحرف الخلاف سمير بسيوني.pdf
مصحف القراءات العشر   أعد أحرف الخلاف سمير بسيوني.pdfمصحف القراءات العشر   أعد أحرف الخلاف سمير بسيوني.pdf
مصحف القراءات العشر أعد أحرف الخلاف سمير بسيوني.pdf
 
Nutrition Inc FY 2024, 4 - Hour Training
Nutrition Inc FY 2024, 4 - Hour TrainingNutrition Inc FY 2024, 4 - Hour Training
Nutrition Inc FY 2024, 4 - Hour Training
 
Electric Fetus - Record Store Scavenger Hunt
Electric Fetus - Record Store Scavenger HuntElectric Fetus - Record Store Scavenger Hunt
Electric Fetus - Record Store Scavenger Hunt
 
Elevate Your Nonprofit's Online Presence_ A Guide to Effective SEO Strategies...
Elevate Your Nonprofit's Online Presence_ A Guide to Effective SEO Strategies...Elevate Your Nonprofit's Online Presence_ A Guide to Effective SEO Strategies...
Elevate Your Nonprofit's Online Presence_ A Guide to Effective SEO Strategies...
 
skeleton System.pdf (skeleton system wow)
skeleton System.pdf (skeleton system wow)skeleton System.pdf (skeleton system wow)
skeleton System.pdf (skeleton system wow)
 
MDP on air pollution of class 8 year 2024-2025
MDP on air pollution of class 8 year 2024-2025MDP on air pollution of class 8 year 2024-2025
MDP on air pollution of class 8 year 2024-2025
 
How Barcodes Can Be Leveraged Within Odoo 17
How Barcodes Can Be Leveraged Within Odoo 17How Barcodes Can Be Leveraged Within Odoo 17
How Barcodes Can Be Leveraged Within Odoo 17
 
BÀI TẬP BỔ TRỢ TIẾNG ANH LỚP 9 CẢ NĂM - GLOBAL SUCCESS - NĂM HỌC 2024-2025 - ...
BÀI TẬP BỔ TRỢ TIẾNG ANH LỚP 9 CẢ NĂM - GLOBAL SUCCESS - NĂM HỌC 2024-2025 - ...BÀI TẬP BỔ TRỢ TIẾNG ANH LỚP 9 CẢ NĂM - GLOBAL SUCCESS - NĂM HỌC 2024-2025 - ...
BÀI TẬP BỔ TRỢ TIẾNG ANH LỚP 9 CẢ NĂM - GLOBAL SUCCESS - NĂM HỌC 2024-2025 - ...
 
The basics of sentences session 7pptx.pptx
The basics of sentences session 7pptx.pptxThe basics of sentences session 7pptx.pptx
The basics of sentences session 7pptx.pptx
 
NEWSPAPERS - QUESTION 1 - REVISION POWERPOINT.pptx
NEWSPAPERS - QUESTION 1 - REVISION POWERPOINT.pptxNEWSPAPERS - QUESTION 1 - REVISION POWERPOINT.pptx
NEWSPAPERS - QUESTION 1 - REVISION POWERPOINT.pptx
 
RESULTS OF THE EVALUATION QUESTIONNAIRE.pptx
RESULTS OF THE EVALUATION QUESTIONNAIRE.pptxRESULTS OF THE EVALUATION QUESTIONNAIRE.pptx
RESULTS OF THE EVALUATION QUESTIONNAIRE.pptx
 
Bonku-Babus-Friend by Sathyajith Ray (9)
Bonku-Babus-Friend by Sathyajith Ray  (9)Bonku-Babus-Friend by Sathyajith Ray  (9)
Bonku-Babus-Friend by Sathyajith Ray (9)
 
Mule event processing models | MuleSoft Mysore Meetup #47
Mule event processing models | MuleSoft Mysore Meetup #47Mule event processing models | MuleSoft Mysore Meetup #47
Mule event processing models | MuleSoft Mysore Meetup #47
 
CIS 4200-02 Group 1 Final Project Report (1).pdf
CIS 4200-02 Group 1 Final Project Report (1).pdfCIS 4200-02 Group 1 Final Project Report (1).pdf
CIS 4200-02 Group 1 Final Project Report (1).pdf
 
Beyond Degrees - Empowering the Workforce in the Context of Skills-First.pptx
Beyond Degrees - Empowering the Workforce in the Context of Skills-First.pptxBeyond Degrees - Empowering the Workforce in the Context of Skills-First.pptx
Beyond Degrees - Empowering the Workforce in the Context of Skills-First.pptx
 
How to Predict Vendor Bill Product in Odoo 17
How to Predict Vendor Bill Product in Odoo 17How to Predict Vendor Bill Product in Odoo 17
How to Predict Vendor Bill Product in Odoo 17
 
Educational Technology in the Health Sciences
Educational Technology in the Health SciencesEducational Technology in the Health Sciences
Educational Technology in the Health Sciences
 
Geography as a Discipline Chapter 1 __ Class 11 Geography NCERT _ Class Notes...
Geography as a Discipline Chapter 1 __ Class 11 Geography NCERT _ Class Notes...Geography as a Discipline Chapter 1 __ Class 11 Geography NCERT _ Class Notes...
Geography as a Discipline Chapter 1 __ Class 11 Geography NCERT _ Class Notes...
 

Life Cycle Management of Computerized System.pdf

  • 1. LIFE CYCLE MANAGEMENT OF COMPUTERIZED SYSTEM RAKTIM DEY DY. MANAGER-VALIDATION AND QUALIFICATION GRANULES INDIA LIMITED
  • 2. OVERVIEW Life cycle management of Computerized system consists of the following major steps: • Requirements • Development • Validation • Implementation/Deployment • Control • Maintenance and • Retirement
  • 3. COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART Change Control Initiation Initial Risk Assessment System Information Business Requirement GXP Relevance ER/ES Relevance GAMP Categorization New System or Existing System or Laboratory software or Production Equipment related or Other control system or etc. User Requirement Specification (URS) • Purpose of the system • Brief description of the system • Design and Environment • Regulatory requirements • Service Requirement • References 1 2 3
  • 4. COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART Vendor Identification and Assessment Identification of Suitable vendor Vendor assessment through audits as applicable Finalization of the vendor Vendor documents DS/FS/CS/operation manual Assessment Validation Plan Validation plan explains about how the necessary requirements will be fulfilled. It will provide the list of life cycle documentation, role and responsibility and define testing strategy, criteria for final acceptance, release of system and maintenance of lifetime compliance. Validation of computerized system shall be performed in a logical, systematic manner and risk based approach shall be followed. 4 5
  • 5. COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART System Installation Qualification Type of Environment – Validation Server or Production Server System Details like Software name, Version, Installation Checklist (Installation of Instrument/Equipment, Installation and Configuration of Application Software Verification of Pre-Installation Checklist (PO, Intactness of system components, etc.) Deviation record, if any. 6
  • 6. COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART System Installation Qualification Type of Environment – Validation Server or Production Server System Details like Software name, Version, Installation Checklist (Installation of Instrument/Equipment, Installation and Configuration of Application Software Verification of Pre-Installation Checklist (PO, Intactness of system components, etc.) Deviation record, if any. Summary and conclusion 7
  • 7. COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART System Operation Qualification Roles of different personnel involved in the qualification of system Reference documents to perform OQ Test Planning [Test Items, Components and functions to be tested] Test Strategy [Test Objective, Test Approach, Recording of results, Acceptance criteria] Deviation record, if any Summary and conclusion 8
  • 8. COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART System Performance Qualification Roles of different personnel involved in the qualification of system Reference documents to perform PQ Test Planning [Test Items, Components and functions to be tested] Test Strategy [Test Objective, Test Approach, Recording of results, Acceptance criteria] Deviation record, if any Summary and conclusion 9
  • 9. COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART Validation Summary Report Objective: The objectives of this VSR are to summarize the results of the validation effort for <Computerized system> to show that the system is validated according to standards and applicable regulatory requirements. Deviations from the Validation Plan, if any Follow up actions w.r.t the deviations Summary and Assessment of System Life Cycle Documentation, e.g. Name Document ID User requirement Specification To record Initial Risk Assessment To record Validation Plan To record Function Specification To record Traceability Matrix To record Risk Assessment (FMECA) To record Post Implementation review, System acceptance and release 10
  • 10. COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART Traceability Matrix URS ID URS specification or Parameter IQ test ID OQ test ID PQ test ID Remarks If any URS-01 URS-02 URS-03 URS-04 Traceability matrix outline the User Requirement and the section in which that particular requirement is tested. 11
  • 11. COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART Post Implementation Review Validation Documents Review Deviation/Change Record Review Audit Trail Record Review System Security and Access Control Review Software and Data Backups Review Training Record Review SOPs Review 12
  • 12. COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART Periodic Review Sr. No. Name of Computerized System Version no. /Release no. Frequency of Review Date of Validation Last Periodic Review done on Next Periodic Review due on Periodic Review done on Periodic Review Report No. Periodic Review of system shall be conducted every year, to assess the continuity of system operation. Any upgradation/Change in the system shall be assessed for re- qualification 13
  • 13. COMPUTERIZED SYSTEM LIFE CYCLE MANAGEMENT FLOWCHART Revalidation Any major Changes/ Upgradation in the system needs to be re-validated. System Retirement Any system which has gone outdated /Non-Functional needs to be obsoleted through proper documentation. A risk assessment may be performed to assess the impact on the particular system retirement on Product/Business continuity/Output etc. 14 15