Jsa Validation Services Baddi (H.P.) India Template of Risk Based Prioritization Plan
Jsa Validation Services Baddi (H.P.) India Template of Risk Based Prioritization Plan
Mitigate
the Risk
Identify
the
Risk
Planing and
Prioritization
JSA VALIDATION SERVICES
BADDI (H.P.) INDIA
TEMPLATE OF RISK BASED PRIORITIZATION PLAN
1. INTRODUCTION :
2. SCOPE :
The risk ranking exercise for prioritizing the QRM is applicable for …………….XYZ Facility.
The prioritizing exercise covers elements as mentioned below:
• Product
• Process
• Equipment
3. ABBREVIATION :
4. REASON FOR REVISION :
Sr. No. Changes Incorporated Reason for changes
5. RESPONSIBILITY :
6. DEFINITITONS :
7. RISK PRIORITIZATION PROCESS :
Formal risk ranking is based on well-defined analytical processes and enhances the quality, transparency, and,
potentially, the performance of risk management programs.
The risk ranking procedure uses an analytical process to pose a risk question; Identify potential hazards and risks;
characterize factors that can be used as variables for quantifying risk; and mathematically combine the variables to
yield an overall risk score for risk ranking.
The overall process is schematically outlined in below mentioned Figure.
For complex
Identify and List all
system s, categorize
Risk Factors
risk factors logically,
(Variables)
administratively etc.
Yes End
Product Factors pertaining to the intrinsic properties of drug Dosage form; intrinsic chemical properties,
products /Intermediates/API such that quality deficiencies highly potent molecules, , key starting
could potentially and adversely impact public health. materials
Facility & Factors relating to characteristics of a manufacturing site Poor cGMP compliance
Equipment believed to be predictive of potential quality risks, such
as the lack of effective quality systems. History, Complaints received suggesting
Class I or Class II health hazard situations
Process Factors pertaining to aspects of drug manufacturing Cleaning Procedures, Processing &
operations that may predict potential difficulties with Controls, Environmental controls &
process control and/or vulnerability to various forms of Management, compression; Cartoning /
contamination. packaging, etc.
QRM initiatives
Utility equipment’s Level of automation & Processing and controls High Cost Products
Alarm Management
Packing machines Distribution Mgmt. High Volume Products
Control storage area
Detection and scanning Maintenance Mgmt.
devices Environmental Controls
& Management Waste Management
Monitoring and
recording devices FP Transportation Mgmt.
Printed Packaging
Material Handling
A Site Risk Potential (SRP) is a function of the weighted risk potentials for each of the categories, Product, Facility
and Process & Equipment. The risk potential for each top-level component is, in turn, a function of select potential
risk factors. Thus, a SRP score is derived by mathematical combination of weights or ranks assigned to select
potential risk factors. The assignment of weights or ranks to select potential risk factors is based on either
empirical evidence or expert judgement or combination of both.
9.1 Quality risk indicators :
Quality risk indicators are top level components for risk based prioritization which include:
▪ Facility & Equipment
▪ Product
▪ Process
9.2 Risk scoring criteria :
Individual risk factors are rated from 1 to 3 with increasing level of priority and total risk score is calculated by
summing individual risk factor values. Based upon individual risk score, particular risk items are ranked.
Three point risk scale are depicted in the table as described below:
Equal to 1 (Minor) The color of the cell in risk rating table is shown as green
Equal to 2 (Major) The color of the cell in risk rating table is shown as yellow
Equal to 3 (Critical) The color of the cell in risk rating table is shown as Red
vulnerable to contamination
Is there a history of product
batches), Interruption of
(Item in red
, to next product)
font indicates
product quality
product
ranked amongst
first five in
product risk
factors)
Sr
No
Total Score
Risk Rank
(0.1 mg)
Risk score 3 Very High >=10 More More than Therapeutic dose
difficult concern than 3 300 batches <100 µg (0.1 mg)
events
Product being
manufactured
at <Plant>
to contamination from
operation in a state of
in control philosophy
of the final product?
How difficult is it to
previous product?
maintain this unit
the environment?
The equipment is
that they are
control?
rank among
first five in
product risk
Total Score
Risk Rank
Risk score 2 Moderate to Moderately Moderately Moderately Moderately Moderately
high Complex difficult reliable vulnerable vulnerable
Risk score 3 Very high High Very Slightly Very Very
Complex difficult reliable vulnerable vulnerable
Processing Equipment
1
2
Packaging Equipment
3
4
Detection, inspection and scanning Equipment
5
6
Utility Equipment
7
8
9
Summary of conclusion
Total Score
Risk Rank
difficult
2= Moderate to 2 =Moderately 2 = Moderately 2 = Moderately vulnerable
high difficult reliable
3 = Very high 3 = Very difficult 3 = Slightly 3 = Very vulnerable
reliable
1 Cross
contamination &
Mix UP
2 Raw Material and
Printed packing
material handling
& controls
3 Cleaning
procedure
4 Maintenance
Management
5 Waste
Management
6 Environment
control &
Management
7 Finished product
transportation
Management
8 Security
Assurance
Summary of rating:
Risk Prioritization
items