SlideShare una empresa de Scribd logo
1 de 13
Presents by
Mr. Nilesh Utpure
Under the guidance of
Miss. Gurjar P. N.
Sharadchandra Pawar College of Pharmacy (otur) Pune-412409
Validation
 Key process for effective quality assurance
 Establishes the documented evidence provide high
degree of assurance
 To check process/ equipment that used to produce
product/ result
 Used to produce the product at its predetermined
specification & quality attribute
2
Objectives of Process Validation
 Software verification & validation
 Describes the program inspection process & its role in
verification & validation
 Describes clean room software development
 Explain static analysis as a verification technique
3
Importance of Process Validation
 Government regulation
 Rapid automation
 Improved employee awareness
 Increased output
 Reduction in quality cost
 Process optimization
4
Purpose & Responsibilities
 To describe the procedure for validation of machine
which ensures that it meet installation, operational &
performance qualification requirements
 It is the responsibility of the production manager &
technical service manager
 The QA manager is responsible for SOP compliance
5
User Requirement Specification
(USR)
 Should be treated as contractual document
 It should be minimum & cover all mandatory parts
including those necessary to guarantee the final
product quality & achieve compliance with rules
 Ideally, requirements should be independent from the
suppliers product & express the customer needs
without addressing specific design solutions
6
URS Scope
 It should be not limited to
1. Level 1 –full details of end user operability
2. Level 2 –full details of functionality
3. Level 3 –software functionality interface
4. Full description of the required system performance
5. Documentation requirements
6. Training requirements
7
Steps involved in life cycle
 Design qualification (DQ)
 Installation qualification (IQ)
 Operational qualification (OQ)
 Performance qualification (PQ)
8
Types of packaging machine
 Strip packaging
 Blister packaging
 Aluminum packaging
9
Detailed assembly
 Unwinding station
 Heating station
 Forming station
 Cooling station
 Feeding station
 Sealing station
 Cooling station
 Labeling station
10
Parameters
 Speed
 Heating
 Punching
 Cooling
 Printing
11
Validation SOP
SOP No. Val: Effective Date:
Approved By:
TITLE: Blistering Machine
Author: _____________________
Name/ Title/ Department Signature
Checked By: _____________________
Name, Title/ Department Signature
Approved By: _____________________
Name/ Title/ Department Signature
Revisions:
No. Section Pages Date
1
2
12
13

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validation of blister packaging machine

  • 1. Presents by Mr. Nilesh Utpure Under the guidance of Miss. Gurjar P. N. Sharadchandra Pawar College of Pharmacy (otur) Pune-412409
  • 2. Validation  Key process for effective quality assurance  Establishes the documented evidence provide high degree of assurance  To check process/ equipment that used to produce product/ result  Used to produce the product at its predetermined specification & quality attribute 2
  • 3. Objectives of Process Validation  Software verification & validation  Describes the program inspection process & its role in verification & validation  Describes clean room software development  Explain static analysis as a verification technique 3
  • 4. Importance of Process Validation  Government regulation  Rapid automation  Improved employee awareness  Increased output  Reduction in quality cost  Process optimization 4
  • 5. Purpose & Responsibilities  To describe the procedure for validation of machine which ensures that it meet installation, operational & performance qualification requirements  It is the responsibility of the production manager & technical service manager  The QA manager is responsible for SOP compliance 5
  • 6. User Requirement Specification (USR)  Should be treated as contractual document  It should be minimum & cover all mandatory parts including those necessary to guarantee the final product quality & achieve compliance with rules  Ideally, requirements should be independent from the suppliers product & express the customer needs without addressing specific design solutions 6
  • 7. URS Scope  It should be not limited to 1. Level 1 –full details of end user operability 2. Level 2 –full details of functionality 3. Level 3 –software functionality interface 4. Full description of the required system performance 5. Documentation requirements 6. Training requirements 7
  • 8. Steps involved in life cycle  Design qualification (DQ)  Installation qualification (IQ)  Operational qualification (OQ)  Performance qualification (PQ) 8
  • 9. Types of packaging machine  Strip packaging  Blister packaging  Aluminum packaging 9
  • 10. Detailed assembly  Unwinding station  Heating station  Forming station  Cooling station  Feeding station  Sealing station  Cooling station  Labeling station 10
  • 11. Parameters  Speed  Heating  Punching  Cooling  Printing 11
  • 12. Validation SOP SOP No. Val: Effective Date: Approved By: TITLE: Blistering Machine Author: _____________________ Name/ Title/ Department Signature Checked By: _____________________ Name, Title/ Department Signature Approved By: _____________________ Name/ Title/ Department Signature Revisions: No. Section Pages Date 1 2 12
  • 13. 13