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Batch Documentation Review & Evaluation
A Last Opportunity to Whistle
Roohi B. Obaid
05th Oct 2019, Karachi
It reflects the views and understanding of presenter
& may not be construed to represent the views or
policies of organization or association to which
speaker has ties
Documents of US-FDA, Papers from
Pharmaceutical Technology & Review Scientific
Articles are used to construct presentation
Oliver Wolf, April 2017
Disclaimer
Reference
Batch history is
imperative to tracking,
sustaining product
quality, viability &
safety
It’s a high risk data
It’s a matter of
life & lives
Check Verify Review
Standard Operating Procedure
Scope
The purpose of documentation is limited to tracking and tracing
the operation
(describe reason for both):
Yes No
Why do we review Batch Record?
Why we do not believe on real time data?
Why do we review Batch Record?
Why we do not believe on real time data?
Why do we review Batch Record?
What we expect from Batch Record Review?
How it is performed?
Lets have a hypothesis outline to make decision
clear & consistent
Minor
health or
regulatory
suffering
Reversible
life crisis
Irreversible
life crisis
Limited to discussion on today’s session
2
1
3
Certificate of Analysis of API
Review
Dispensing Document Review
Dispensing Document Review
Dispensing Document Review
A
Dispensing Document Review
L
Dispensing Document Review
C
Dispensing Document Review
O
Dispensing Document Review
A
Dispensing Document Review
Complete
Dispensing Document Review
Consistent
Dispensing Document Review
Enduring
Dispensing Document Review
Available
Supplier
Program1
Personnel
Training 2
Instrument
Qualification3
Environment
Monitoring4
Validation
Practices 5
Change
Management6
Granulation Document Review
Granulation Document Review
Granulation Document Review
A
Granulation Document Review
L
Granulation Document Review
C
Granulation Document Review
O
Granulation Document Review
A
Granulation Document Review
Complete
Granulation Document Review
Consistent
Granulation Document Review
Enduring
Granulation Document Review
Available
Supplier
Program1
Personnel
Training 2
Instrument
Qualification3
Environment
Monitoring4
Validation
Practices 5
Change
Management6
Compression & Packaging
Document Review
Compression & Packaging
Document Review
Compression & Packaging
Document Review
A
Compression & Packaging
Document Review
L
Compression & Packaging
Document Review
C
Compression & Packaging
Document Review
O
Compression & Packaging
Document Review
A
Compression & Packaging
Document Review
Complete
Compression & Packaging
Document Review
Consistent
Compression & Packaging
Document Review
Enduring
Compression & Packaging
Document Review
Available
Supplier
Program1
Personnel
Training 2
Instrument
Qualification3
Environment
Monitoring4
Validation
Practices 5
Change
Management6
Bulk Holding Document Review
Bulk Holding Document Review
Bulk Holding Document Review
A
Bulk Holding Document Review
L
Bulk Holding Document Review
C
Bulk Holding Document Review
O
Bulk Holding Document Review
A
Bulk Holding Document Review
Complete
Bulk Holding Document Review
Consistent
Bulk Holding Document Review
Enduring
Bulk Holding Document Review
Available
Supplier
Program1
Personnel
Training 2
Instrument
Qualification3
Environment
Monitoring4
Validation
Practices 5
Change
Management6
Testing Document Review
Testing Document Review
Testing Document Review
A
Testing Document Review
L
Testing Document Review
C
Testing Document Review
O
Testing Document Review
A
Testing Document Review
Complete
Testing Document Review
Consistent
Testing Document Review
Enduring
Testing Document Review
Available
Supplier
Program1
Personnel
Training 2
Instrument
Qualification3
Environment
Monitoring4
Validation
Practices 5
Change
Management6
Commonly recorded errors
Documentation not
contemporaneous
Handwritten change but
date of change was not
traceable
Use of ditto mark
Use of signature stamp
Ink color is not
specified & multi color
is used without reason
Log book correction
failed to identify the
person who made the
change
Use of pencil
Traces of erasing pencil
marks
Inaccurate record copied
Meta data not available
for verification
Correction of
documentation error
should include
Correction of
documentation error
should include
Draw a single line through the error1
Correction of
documentation error
should include
Draw a single line through the error
Make the correction next to the error2
1
Correction of
documentation error
should include
Draw a single line through the error
Make the correction next to the error
Write an explanation for the error
2
1
3
Correction of
documentation error
should include
Draw a single line through the error
Signature & date the correction
Make the correction next to the error
Write an explanation for the error
2
1
4
3
Batch Record Challenges
Manual recording are
inherently slow & prone
to error
Manual recording are
inherently slow & prone
to error
Incorrect data entry
Manual recording are
inherently slow & prone
to error
Blindness & failure to recognize OOS
Incorrect data entry
Manual recording are
inherently slow & prone
to error
Blindness & failure to recognize OOS
Missing signatures
Incorrect data entry
Manual recording are
inherently slow & prone
to error
Blindness & failure to recognize OOS
Missing signatures
Used incorrect form
Incorrect data entry
Manual recording are
inherently slow & prone
to error
Blindness & failure to recognize OOS
Sending wrong form to wrong person
Missing signatures
Used incorrect form
Incorrect data entry
Manual recording are
inherently slow & prone
to error
Blindness & failure to recognize OOS
Sending wrong form to wrong person
Missing signatures
Used incorrect form
Incorrect data entry
Form left incomplete
Data located in separate
positions
What documentation was missed & what
reviews missed. List the deficiencies
Pakistan
150 deaths case
Thank You

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Documentation & Batch Documentation Review - Oct 2019