Validation Part7
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Transcript of Validation Part7
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Validation | Slide 1 of 35 August 2006
Validation
Supplementary Training Modules on Good Manufacturing Practice
WHO Technical Report Series, No. 937, 2006. Annex 4.
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Validation | Slide 2 of 35 August 2006
ValidationValidation
Part 1. General overview on qualification and validation
Part 2. Qualification of HVAC and water systems
Part 3. Cleaning validation
Part 4. Analytical method validation
Part 5. Computerized system validation
Part 6. Qualification of systems and equipment
Part 7. Non sterile product process validation
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Validation | Slide 3 of 35 August 2006
Non sterile product process validation
Part 7
Supplementary Training Modules on Good Manufacturing Practice
WHO Technical Report Series, No. 937, 2006. Annex 4. Appendix 7.
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Validation | Slide 4 of 35 August 2006
ValidationValidation
Objectives
To discuss non-sterile process validation, focusing on:
General recommendations
Prospective validation
Concurrent validation
Retrospective validation
Revalidation
Change control
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ValidationValidation
Principle
Documented evidence: Process is capable of reliably and repeatedly rendering a product of the required quality
Planning, organizing and performing process validation
Process validation protocols
Data collected and reviewed against predetermined acceptance criteria – recorded in validation report
1.1 – 1.2
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ValidationValidation
Scope
General aspects of process validation for the manufacture of non-sterile finished products
Should cover at least the critical steps and parameters, i.e. those that may have an impact on the quality of the product
2.1 – 2.2
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Validation | Slide 7 of 35 August 2006
ValidationValidation
General
Policy and approach to be documented– e.g. in a validation master plan – including critical process
steps and parameters
Process validation to start after qualification of support systems and equipment is completed
In some cases - concurrently with PQ– Normally completed prior to the manufacture of finished
product that is intended for sale (prospective validation)– During routine production (concurrent validation)
3.1 – 3.3
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Validation | Slide 8 of 35 August 2006
ValidationValidation
Prospective validation
Critical factors or parameters possibly affecting finished product quality to be identified during product development
– Breakdown of production process into individual steps– Evaluate each step
Determine the criticality of these factors through a “worst-case” challenge where possible
4.1 – 4.2
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ValidationValidation
(continued) Prospective validation protocol should include:
– description of the process and of the experiment– equipment and/or facilities to be used including measuring
or recording equipment (and its calibration status)– variables to be monitored– details of the samples to be taken– product performance characteristics/attributes to be
monitored, together with the test methods– acceptable limits and time schedules– personnel responsibilities– details of methods for recording and evaluating results,
including statistical analysis 4.3
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ValidationValidation
Approach:
Equipment, production environment and analytical testing methods – already fully validated
– e.g. during installation qualification and operational qualification
Appropriately trained personnel and batch manufacturing documentation prepared after these critical parameters have been identified, and machine settings, component specifications and environmental conditions have been determined and specified
4.4 – 4.6
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ValidationValidation
Approach (2)
A number of batches of the final product should then be produced
What number of batches?– sufficient to allow the normal extent of variation and trends
to be established and– to provide sufficient data for evaluation
Data within the finally agreed parameters– from at least three consecutive batches, giving product of
the desired quality may be considered acceptable4.7 – 4.8
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ValidationValidation
Approach (3)
Same size batches
Full-scale production batch size– If not possible – reduced batch size considered– Validity of assumptions made should be demonstrated
when full-scale production starts
Extensive testing at various stages in the manufacturing process – including on the final product and its package
4.9 – 4.10
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ValidationValidation
Setting Limits: may include– Marketing authorization limits
stability specifications– Release specification– Validation limits
Batch release limits
Marketing authorization limitsbased on stability specifications
Validation limits
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Validation | Slide 14 of 35 August 2006
Determining critical control point: example of a tablet granulation process
Particle size distribution of the active(s)
Blending time for the powder
Granulating time and speed; amount of granulating fluid and binder concentration
Drying time – final moisture content, granule particle size distribution
Granule active content and homogeneity, blending time of external phase
Validation
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Criticalcontrol
point
Decision as to whether tocompress or not based on
expected yield and actual yield
Process step Operation IQ/OQ/PQ requirements
Criticalcontrolpoint
Measure humidity withhumidity meterXIII
IQ/OQcalibration
Weigh granulate - balanceXIV IQ/OQcalibration
instrumentoperation,
cleaning, careand maintenance
Trainingrecords fortechnician
XV Sieve 3/5
sieve with sieve type 1
XVI Blend3/5
granulatemixer (speed 1, 1 minute)
XVI Blend 2with 3/5
granulate
mixer (speed 1, 30seconds)
IQ/OQ/PQCleaning
validationCleaning, and Blend
uniformity required to beestablished during validation
XVIII Weigh granulate
Validation
Determining critical control points
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Validation | Slide 16 of 35 August 2006
Solid dose mixing (1)
Homogeneity in blending – the key to quality!
Sampling strategy
Sample site, label, container
Storage
Transport
Sample thief
Validation
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Solid dose mixing (2) In situ analysis
Methods of analysis
Statistical analysis – inter-batch
– intra-batch
– within-sample-site
Validation
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ValidationValidation
Tablet compression variables
Fill volume
Pre- and compression force
Turntable speed
Dwell time
Granule size and feed
Ejection force, lubrication
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ValidationValidation
Tablet compressionparameters
Mass
Hardness
Moisture
Friability
Disintegration
Dissolution Thickness
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ValidationValidation
Tablet coating variables Spray rate Inlet and outlet air temp Coating weight
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ValidationValidation
Results in the report that includes, e.g.– process description including details of critical steps– detailed summary of the results obtained from in-process
and final testing, including data from failed tests– raw data or reference to these– any work done in addition to that specified in the protocol– any deviations from the protocol with an explanation– a review and comparison of the results with those expected– formal acceptance or rejection of the work by the team or
persons designated as being responsible for the validation, after completion of any corrective action or repeated work
4.11
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ValidationValidation
Conclusion and recommendation:– Made on the basis of the results obtained– Incorporated into the batch manufacturing and batch
packaging documents and/or standard operating procedures (SOPs) for routine use
– Limits and frequencies of testing and monitoring should be specified. Actions in case of OOL
If validation batches are to be sold or supplied:– manufactured under GMP conditions– Compliance with the marketing authorization
4.12. – 4.14.
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ValidationValidation
Concurrent validation
May be appropriate to validate a process during routine production
– Can you give any examples?
Decision made by appropriately authorized personnel
Premises and equipment previously qualified
Done as per validation protocol; and results documented in the validation report
5.1 – 5.5
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ValidationValidation
Retrospective validation
Comprehensive review of historical data
Requires a protocol and a report with a conclusion and a recommendation
Not the preferred method of validation, and used in exceptional cases only:
– e.g. for well-established processes
Inappropriate in case of changes (e.g. equipment)
6.1 – 6.2
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ValidationValidation
Retrospective validation (2)
Sufficient data to be reviewed to provide a statistically significant conclusion
Satisfactory results of retrospective validation
only serve as an indication
that the process does not need
to be subjected to validation
in the immediate future6.3 – 6.4
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ValidationValidation
Revalidation
Standard processes (with conventional equipment)– data review similar to retrospective validation
Points to be considered:– the occurrence of any changes in the master formula,
methods, starting material manufacturer, equipment and/or instruments
– calibrations and preventive maintenance carried out– standard operating procedures (SOPs)– cleaning and hygiene programme
7.1
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ValidationValidation
Change control In case of changes, consider the change and its impact on the
process validation
Examples of changes (requiring revalidation):– manufacturing process (e.g. mixing times, drying
temperatures)– equipment (e.g. addition of automatic detection systems)– production area and support system changes– transfer of processes to another site– unexpected changes (e.g. those observed during self-
inspection or during routine analysis of process trend data)8.1 – 8.2
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Validation | Slide 28 of 35 August 2006
Validation
Non sterile products
Tablets
Capsules Creams
Ointments
Suspensions Syrups
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ValidationValidation
Non sterile products
List some of the key parameters to be considered in the process validation of the dosage forms mentioned
2.4
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Validation | Slide 30 of 35 August 2006
Validation
SUMMARYProspective validation
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Validation
SUMMARYProspective validation
Concurrent validation
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Validation | Slide 32 of 35 August 2006
Validation
SUMMARYProspective validation
Concurrent validation
Retrospective validation
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Validation
SUMMARYProspective validation
Concurrent validation
Retrospective validation
Revalidation
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Validation | Slide 34 of 35 August 2006
Validation
SUMMARYProspective validation
Concurrent validation
Retrospective validation
Change control
Revalidation
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Validation | Slide 35 of 35 August 2006
Validation
Group Session
You are given a tablet manufacturing flow chart to study
List the critical steps that are required to be validated
List the critical equipment required to be qualified
Identify the variables and construct a table as directed