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Module 1, Part 1: Introduction and The VMP Slide 1 of 22 © WHO – EDM
Validation
Supplementary Training Modules on Good Manufacturing Practices
Module 1, Part 1: Introduction and The VMP Slide 2 of 22 © WHO – EDM
Part I: Introduction and The Validation Master Plan
(VMP)Part 2: Cleaning validationPart 3: Process validationPart 4: QC-related validationPart 5: Review and summary
Validation
Module 1, Part 1: Introduction and The VMP Slide 3 of 22 © WHO – EDM
Objectives of Part 1 To provide an introduction to the subject
of Validation To provide information on the Validation
Master Plan
Validation
Module 1, Part 1: Introduction and The VMP Slide 4 of 22 © WHO – EDM
Validation
IntroductionThree basic principles of Quality
Assurance: Quality, safety, effectiveness Cannot inspect quality into a product Processes must be under control
Module 1, Part 1: Introduction and The VMP Slide 5 of 22 © WHO – EDM
Validation
WHO validation definition The documented act of proving that any
procedure, process, equipment, material, activity, or system actually leads to the expected results.
Module 1, Part 1: Introduction and The VMP Slide 6 of 22 © WHO – EDM
Qualification or validation?
A system must be qualified to operate in a validated process
Qualify a system and/or equipment Validate a process Qualification versus validation, e.g. you
qualify an autoclave, whereas you validate a sterilization process
Validation
Module 1, Part 1: Introduction and The VMP Slide 7 of 22 © WHO – EDM
Qualification and validation work require:
Collaboration of experts
Budget
Meticulous and careful planning
A Validation
Master Plan helps
the manufactur
er and inspectorat
e
Validation
Module 1, Part 1: Introduction and The VMP Slide 8 of 22 © WHO – EDM
Validation The Validation Master
Plan (VMP)
Philosophy Content Strategy
Module 1, Part 1: Introduction and The VMP Slide 9 of 22 © WHO – EDM
Validation
Validation Master Plan Recommendation only Cover manufacturer’s validation policy and needs
Provides information on validation
organization It should describe:
why? what? where?
by whom? how? when?
Module 1, Part 1: Introduction and The VMP Slide 10 of 22
© WHO – EDM
Validation
Validation Master Plan Prospective validation Concurrent validation Retrospective validation Revalidation Change control
Module 1, Part 1: Introduction and The VMP Slide 11 of 22
© WHO – EDM
Validation
The VMP helps: Management Validation team members Project leaders GMP inspectors
Module 1, Part 1: Introduction and The VMP Slide 12 of 22
© WHO – EDM
Validation
The VMP Identifies validation items (products,
processes, systems) Defines nature and extent of testing
expected Outlines test procedures and protocols Summary document Management agreement
Module 1, Part 1: Introduction and The VMP Slide 13 of 22
© WHO – EDM
Validation Activities in VMP Every validation activity included Revalidation Validation of new process cycles Large validation projects have separate VMPs Include reasonable unexpected events
Validation
Module 1, Part 1: Introduction and The VMP Slide 14 of 22
© WHO – EDM
Validation
The VMP: Enables overview of entire validation
project Lists items to be validated with the
planning schedule as its heart Is like a map
Module 1, Part 1: Introduction and The VMP Slide 15 of 22
© WHO – EDM
Validation
The “Introduction” to the VMP Validation policy Project scope Location and timing (including priorities) Validation procedures Standards
Module 1, Part 1: Introduction and The VMP Slide 16 of 22
© WHO – EDM
ValidationVMP should state who is responsible for: Preparing the VMP The protocols and SOPs Validation work Report and document preparation and control Approval/authorisation of validation protocols
and reports in all stages of validation process Tracking system Training needs in support of validation
Module 1, Part 1: Introduction and The VMP Slide 17 of 22
© WHO – EDM
Validation
VMP should contain: Cross references to documents Specific process considerations Specific characteristics briefly outlined Validation list (What to validate)
premises, systems and equipment processes products
Module 1, Part 1: Introduction and The VMP Slide 18 of 22
© WHO – EDM
ValidationVMP should contain: Descriptions of
plant (where to validate) processes products
Personnel attributes expertise and training
Key acceptance criteria
Module 1, Part 1: Introduction and The VMP Slide 19 of 22
© WHO – EDM
VMP should contain: Format for protocols and other
documentation List of relevant SOPs (How) Planning and scheduling (When) Location (Where) Estimate of staffing requirements (Who) A time plan of the project (When) Annexes
Validation
Module 1, Part 1: Introduction and The VMP Slide 20 of 22
© WHO – EDM
Validation
VMP should contain change control Policy and procedure Risk assessment Authorization Failure to properly document changes to the
system means invalidation of the process
Module 1, Part 1: Introduction and The VMP Slide 21 of 22
© WHO – EDM
Validation
Changes that require revalidation Software changes; Controllers Site changes; Operational changes Change of source of material Change in the process Significant equipment change Production area changes Support system changes
Module 1, Part 1: Introduction and The VMP Slide 22 of 22
© WHO – EDM
Validation
In summary, a VMP should contain atleast: Validation policy Organizational structure Summary of facilities, systems, equipment,
processes to be validated Documentation format for protocols and
reports Planning and scheduling Change control Training requirements