Deviation and OOS Handling

Dr.
J rgen Mhlitz Slide 1 District Government of Swabia

Deviation and
Out of Specification Handling
Dr. J rgen Mhlitz
GMP Inspector
District Government of Swabia
Fronhof 10
D-86152 Augsburg
Germany
APV Training Course
GMP Requirements
J une,10th to11th 2004
Istanbul, Turkey
6/13/2004
Failure Investigations,
Inspectors Expectations
Dr. J rgen Mhlitz Slide 3 District Government of Swabia
Topics to be Covered
Legal background
Expected Content of Deviation
Report
Where Companies Have Difficulty
Example Citations
Summary
References
Governing Authority, EU
Commission Directive 2003/94EC
(replaces 91/356/EEC)
All process deviations and product
defects shall be documented and
thoroughly investigated
(Article 10, Production)
Governing Authority, EU
EC Guide to Good Manufacturing
Practice, Chapter 5 (5.15)
Any deviations from instructions or
procedures should be avoided as far as
possible. If a deviation occurs, it should
be approved in writing by a competent
person
Governing Authority, US
21 CFR 211.192 and Multiple Other
Provisions within 211
Any unexplained discrepancyshall
be thoroughly investigatedThe
investigation shall extend to other
batches that can have been
associated with the specific failure or
discrepancy. A written record of the
investigation shall be made and shall
include the conclusions and follow-up.
Governing Authority
ICHQ7A, GMPs for Active
Pharmaceutical Ingredients
Any deviation from established procedures
should be documented and explained.
Critical deviations should be investigated, and
the investigation and its conclusions should
be documented.
All deviation, investigation and OOS reports
should be reviewed as part of the batch
record review before the batch is released.
U.S. Legal Opinion
United States v Barr Laboratories, Inc.
1993 Described Requirements for
Investigations
Specifies Content of Failure Report;
Requires Listing and Evaluation of Lots
Potentially Affected;
Elements of Thoroughness Vary Depending
on Nature and Impact of the Event;
Defines Promptly as 30 days from Event
Linkage of Systems
EVENT
Investigation
Corrective Action
Preventive Action
Root Cause
Identify All Lots
Consider All Possibilities
Product Impact
Lot Disposition
Definition of Deviation
Departure from Written Instructions,
Unexpected Event,
Departure from cGMP;
Identify Exempted Incidents, Generally
Documentation
Multiple Systems Can be Problematic
Create Confusion and Difficult to Track
Minimize Notes or Comments
Many Should be Deviations with Abbreviated
Investigations
Scope and Definition
Scope and Definition
Purpose of Investigations
Identify
Correct
Evaluate Product Impact / Disposition
Prevent Similar Events from Happening
in the Future;
The Deviation Event is the Initiating
Feature of the CAPA Program
Content of Investigation Report
Reason for the Investigation
What Event or Finding Prompted Investigation
How and When Identified
Remember to Consider Tracking / Trending
Evaluation
Consider Related Activities, Think Global
Describe What Happened
When
Where
What Immediate Actions Were Taken
Identify Other Batches Potentially
Affected
Justify Selection
Remember Distributed Lots
Identify Root Cause, Where Possible
Why, Why, Why
Document Factors Considered
Ensure Data Support Conclusions
Avoid Conjecture
Often a Multi-Disciplinary Exercise
Identify Corrective Actions
Resist: Operator Error Corrected with
Retraining
May Include Additional Monitoring /
Assessment
Implementation Must be Timely
Identify Preventive Actions
Success Depends on Adequate Identification
of Root Cause
Interim Solution May Include Additional
Monitoring
Evaluate Product Impact / Disposition
Additional Testing / Results
Justify Accept / Reject Criteria
Justify if Differences in Lot Disposition
Remember to Consider Tox Evaluation
Provide Follow-up to Assure
Effectiveness
Does Preventive Action Provide a Durable
Fix
What are Criteria for Durable Fix
Where are the Deficiencies?
Lack of Documented Investigation
Incomplete Investigation
Factors Not Considered / Documented
Associated Lots Not Identified / Evaluated
Root Cause Not Established or Justified
Conclusions Not Supported by Data
Timelines Not Followed, Not Extended
Corrective / Preventive Actions Not
Implemented, Tracked or Completed
Effectiveness Not Verified
Operator Error is Not Specific
Operator Action
Inattention to Detail
Verbal or Written Communication Problem
Operator Monitoring Multiple Processes
Operator Training:
Not Trained on Procedure
Not Trained on Current Version of Procedure
Insufficient Practice or Experience
Inadequate Content in Training
Operator Error
Management System
Inadequate Administrative Control
Work Organization / Planning Deficiency
Inadequate Supervision
Improper Resource Allocation
Information Not Adequately Defined,
Disseminated or Enforced
Equipment
Equipment Failure
Calibration Not Current
Multiple Work Order(s) Addressing Same
Issue Didnt Correct Problem
Preventive Maintenance Not Current
Out of Tolerance
Equipment Not Operated According to
Validated Procedure
Defective Part
Improper Part
No IQ/OQ or Inadequate IQ/OQ
Electrical Power Failure or Surge
Summary of Inspector Expectations
Implement and Follow an Adequate
Procedure
Perform and Document Thorough
Investigations and Testing Commensurate
with Event and Potential Impact
Adhere to Time Limits
Identify Other Possibly Affected Lots
Evaluate Impact on Product
Implement and Evaluate Corrective /
Preventive Actions
Quality Unit to Review and Approve
Report and Disposition Product
OOS-Results
Expectations of Monitoring Authorities
OOS-Results
Definition of OOS-Results
Importance of OOS-Results and drug legislation
Expectations of the monitoring authority
Content of an OOS SOP
Frequently asked questions
Surveillance of the release decision
Summary
OOS-Results
Definition
Definition of OOS-Result
Test results, laying outside of the specifications, are OOS-Results.
Specifications cover a tolerance area with limits, in which the result to
be determined should be.
These limits may be numerical without dimensions as well as
numerical with dimensions.
Also terms like complies, not more than, more or less colored than
or other terms from official test procedures are allowed limits.
OOS-Results
Specifications may be fixed in or may be diverted from:
official pharmacopoeia (Ph. Eur., DAB, - any other national
pharmacopoeia of an EC member state or those from third
countries, e.g. USP)
registration files
old registration documentation
standard marketing authorization documentation
any other product- or sample specific documentation
OOS-Results:
Scope 1
Scope 1
Investigations of "OOS-results" have to be done in cases of
batch release testing and testing of excipients .
API, excipients in-process control final product
?
Is an investigation of IPC OOS results really necessary?
Will those IPC data be transferred to batch release certificates?
If yes, IPC-testing has to be covered by OOS procedures.
OOS-Results:
Scope 2
Scope 2
Are there other domains that require an investigation in case of OOS
results?
- Stability studies on marketed batches of finished products and or
active pharmaceutical ingredients, ongoing / follow up stability (no
stress tests)
-Previous released batch used as reference sample in an OOS
investigation showing OOS or suspect results
-Batches for clinical trails
OOS-investigation is necessary
Recall of the potentially defective product may be indicated
Example
Example: Reference sample with suspect results
Assay: 93,5 % Mixed sample of batch No. 015 (beginning, middle
and of production)
93,7 % first retest
OOS-investigation: no obvious laboratory failure
no failure in sampling, sample transport and storage
no conspicuous remarks in the batch protocol
2. Retest of batch No. 15, using batch No. 14 as a reference sample with known
content (batch No. 014, assay of batch release testing: 96,8 % ):
Results of the 2. retest:
batch 015: 97,4 % in spec
batch 014: 101,2 % in spec ????
Obvious laboratory failure?
Batch release of batch No. 15? Further investigation necessary!
OOS-Results:Written procedures
What is expected by the inspectorate?
A QA-system with written procedures for e.g.:
Equipment: maintenance, calibration, documentation
Reference materials: CRS, in-house standards,
Sampling
Testing:
sample preparation sample sequence calculations
acceptance criteria
Trends
Release decision
...
OOS-Results
OOS-Results:
SOP on Sampling
SOP on sampling
The amount of the sample taken should be sufficient for
the initial test sequence
investigation
confirmation of the OOS-results
retain sample
A lack of sample material is not a suitable reason for
resampling during an OOS investigation
OOS-Results:
Testing
Testing:
Sample preparation
one or more sample preparations per sample sequence
Sample sequence
number of standard preparations and injections
number of sample preparations and injections
quality control samples
Calculation of the result
definition of result, formula, average
Acceptance criteria for the sample sequence
OOS-Results:OOS-SOP 1
Content and possible structure of an OOS SOP
Definitions
Competent persons to identify an OOS result
Investigation of reasons and conformation of OOS-results:
Laboratory level
Technician/analyst: checklist, obvious laboratory failure?
Head of laboratory: checklist, non obvious laboratory failure?
Raw data check
Written comment of the
head of the laboratory:
Due to an instrument error
the integration with the
lowest standard is a little
bit exotic. The observed
phenomena has no impact
on the analytical results.
OOS-Results: example
Raw data check
0,2 - 16 g/ml
y= -14632 + 227450x
r= 0,9995345
.
0,1 - 20 g/ml
y= -6991 + 323632x + -5976x
r= 0,9999591
HPLC/DAD
calibration curves
day to day
identical standard
material and method
same concentration
no comments
OOS-Results: example
OOS-Results:
OOS-SOP 2
General proceedings for OOS investigations:
Number of reanalysis (same sample preparation)
Number of retests (new sample preparations)
Prolonged sample sequence
Inclusion of a reference sample?
Statistic; average, out layers?
OOS-Results:
OOS-SOP 3
Level of failure investigation:
Laboratory internally
Sampling, sample transport and storage
Batch record review, production
Production process
regulations for cooperation between all involved
departments
OOS-Results:
OOS-SOP 4
Documentation of all OOS investigations and their reports
Evaluation of all OOS-results and investigations
Accumulation of OOS-results for some methods?
Accumulation of OOS-results for some products?
Accumulation of OOS-results for employees?
OOS-Results:
OOS-SOP 5
Timetable for the investigation
inside the laboratory
sampling
production
report / decision
0 - 7 2 - 10 2 - 21 - 30 days
OOS-Results:
OOS-SOP 6
Report after the investigation with establishment for release,
non release or other decision (e.g. reworking)
Follow up?
Change Control?
Flow chart / decision tree with unequivocal decisions:
release or quarantining
OOS-Results
Expectation of the monitoring authority
Quality control unit / qualified person of firm
Mustermann:
A sample for which an OOS-result is confirmed, will be complaint
and the corresponding batch of the
API,
excipient or
finished product
is quarantined.
OOS-Results:FAQ
Frequently asked questions
Are there specifications of a first and second level?
Specifications of new registered products / older registrations
Specifications of products with chemical APIs / herbal
medicines
Determination of physical parameter (pH, hardness) / HPLC-
assay
Safety relevant specifications / process-technical specifications
OOS-Results:FAQ
3AQ11a Specifications and Control Tests on the Finished
Product 1
"The aim of the application dossier for a marketing authorization is
to set the quality level of the medicinal product as intended for
marketing. It establishes specifications, i.e. qualitative and
quantitative characteristics, with test procedures and
acceptance limits, with which the medicinal product must
comply during its intended shelf life.
OOS-Results:FAQ
Product 2
1.4.1
In the marketing authorization dossier, it must be shown that the
manufacturing process used in compliance with GMP is capable
of producing the finished product consistently in compliance
with the specifications chosen;
1.4.2 Routine tests and periodic tests
Different types of tests may exist:
a) tests to be carried out batch by batch on the finished product ... or
bulk
OOS-Results:FAQ
Product 3
b) tests ... on intermediate products or in-process controls will contribute a
greater guarantee of finished product compliance than their
performance on the finished product or on the bulk product;
c) periodic tests ... (e.g. microbiological quality);
d) tests whose performance on the finished product or possibly on the bulk
product at manufacture can be replaced by the verification of another
highly dependent specification (for example replacement of the test for
uniformity of mass with the test for uniformity of content);
OOS-Results:FAQ
Product 4
e) tests which are not carried out routinely once the guarantees of
compliance are furnished by the manufacturer; these specific
cases are exceptional (e.g. identification of colorants);
f ) tests corresponding to critical points in the manufacturing process
to be monitored particularly during the first n production
batches and temporarily in the course of any substantial
modification (for example changing the manufacturing site,
materials, etc.). Subsequently, as a function of acquired
experience and especially validation of the production process,
their batch by batch performance can be omitted (e.g. residual
solvents).
OOS-Results:FAQ
CPMP/QWP/155/96 Note for Guidance on Development
Pharmaceutics
"Properly conducted development studies should ensure that
relevant release and shelf life specifications are applied in order
that the desired characteristics of the product can consistently
be met at release, and throughout shelf life."
OOS-Results:FAQ
Does the competent person has the liberty to interpret the given
specifications?
Development marketing in life phase
authorization
OOS-Results: Release decision 1
Monitoring of the release decision
Regulation on pharmaceutical entrepreneurs (PharmBetrV), based
on the German drug law
6 (2) PharmBetrV: Testing ... has to be done in compliance with
the specifications and limits established in the in the marketing
authorization dossier.
7 (2) PharmBetrV: Finished goods and excipients, not full filling
the requirements have to be
labeled,
quarantined,
destroyed,
resend or
reworked
During routine GMP-inspections the competent authority has to
ensure, that the all legal requirement during production and
release of a batch are met.
Release of a batch, not full filling all specification, has to be
complaint by the competent authority.
"Specifications are critical quality standards that are proposed
and justified by the manufacturer and approved by regulatory
authorities as conditions of approval. (ICH-Topic Q 6 A
Specifications) "
It is not a task of the monitoring authority to evaluate the deviation
from the approved specifications like a second-class licensing
authority.
The evaluation of the health risk is done in cooperation between
monitoring and regulatory authority. Based on that evaluation the
proper and indicated corrective action will be enforced by the
monitoring authority.
OOS-result ... batch relased
medicinal product with significantly reduced quality?
( 8, 96 AMG, 1 year imprisonment).
OOS-result batch released
serious medicinal product with potential risk for the consumer health?
( 5, 95 AMG, 3 J ahre)
OOS-Results:Summary
Every OOS-result in case of release relevant specifications requires
an investigation.
The investigation has to follow a pre established investigation plan.
The investigation has to be summarized in a report .
The report is the basis for a release decision.
All reports have to be documented and evaluated.
If necessary and possible preventative/corrective action has to be
taken.

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What are the legal requirements for investigating deviations and out-of-specification results according to EU and US regulations?

What steps must be included in an investigation of a deviation or out-of-specification result?

Dr.

J rgen Mhlitz Slide 1 District Government of Swabia

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