Question: QUESTION 3 0 According to ICH Q 1 0 , to implement and maintain the pharmaceutical quality system and continually improve its effectiveness, organisations should:
QUESTION
According to ICH Q to implement and maintain the pharmaceutical quality system and continually improve its effectiveness, organisations should:
a
determine and prioritise quality projects for significant step changes
b
determine and develop key individuals as quality champions
c
determine and establish procedures for structured improvement programmes
d
determine and provide adequate and appropriate resources
points
QUESTION
Incidents must be formally reported by a QP
a
False
b
True
points
QUESTION
What is the minimum proving standard for a cleaning validation?
consecutive cleaning applications
consecutive cleaning applications
consecutive cleaning applications
consecutive cleaning applications
points
QUESTION
A clinical trial conducted according to a single protocol at more than one study centre is called a
a
Multiinvestigator study
b
None of these
c
Multicountry study
d
Multi centre study
points
QUESTION
For a Licensed Product, a widening of the specification would be regarded as a Major change
a
False
b
True
points
QUESTION
Continuous improvement is
a
Based on small changes to enhance performance
b
A Kaizen blitz day every month
c
A team building exercise
d
Looking for radical break through enhancements
points
QUESTION
When a company awards a contract to an external, outsourced company which of the following is not true?
The Contract Giver is responsible for assessing the legality, suitability and the competence of the Contract Acceptor
The Contract Giver should monitor and review the performance of the Contract Acceptor
The Contract Acceptor may subcontract to a third party without the Contract Givers approval
The Contract Acceptor should ensure that all products, materials and knowledge provided are suitable for their intended purpose
points
QUESTION
Which of the following would not be found in the Product Specification File?
a
Quality Control testing
b
Shipping details
c
Trial methodology
d
Packaging detail
points
QUESTION
Which of these is used to test the transportation packaging and routes for pharmaceutical distribution?
transport verification
transport validation
transport qualification
transport monitoring
points
QUESTION
The process where a marketed product is placed inside an empty capsule shell and filled with an inert filler to produce a blinded IMP is called
a
None of these
b
Overencapsulation
c
Double dummy manufacture
d
Capsulation
points
QUESTION
Records provide
a
evidence of actions taken
b
All of these
c
demonstrate compliance with instructions
d
raw data
points
QUESTION
Which of these is a disadvantage of active cooling systems used in cold chain logistics to maintain temperature control?
Refrigerant must be conditioned according to spec
Longer pack out times
Cannot be shipped to all destinations
not very secure
points
QUESTION
The starting point for problem solving is
a
To prioritise the best solutions
b
To discover all the causes of the problem
c
To define the problem effect clearly
d
To eliminate erroneous data
points
QUESTION
Incidents nonconformities or deviations should be reported;
a
At the time of the event by anyone
b
To the medicines inspector
c
Immediately to the CEO or Managing Director
d
Only if there is a potentially serious impact on the patient
points
QUESTION
Process equipment must be
a
Stable
b
Validated
c
Randomly used
d
Qualified
points
QUESTION
Continuous improvement activities can be applied to:
a
Process
b
All of these
c
Product
d
Systems
points
QUESTION
Continuous improvement is often a source of motivation as:
a
All of these
b
It promotes involvement
c
It can help reinforce team working
d
It helps encourage workers to take ownership for their work
points
QUESTION
The Fishbone diagram is also referred to as the
a
Ishikawa diagram
b
Kanri management diagram
c
Effect diagram
d
Jidoka diagram
points
QUESTION
Which of the following documents form part of a Product Specification File:
a
Label template
b
Stability test results
c
Manufacturing method
d
All of these
points
QUESTION
The final report of an incident, nonconformity or deviation should be;
a
All of these
b
Clear, conci
Step by Step Solution
There are 3 Steps involved in it
1 Expert Approved Answer
Step: 1 Unlock
Question Has Been Solved by an Expert!
Get step-by-step solutions from verified subject matter experts
Step: 2 Unlock
Step: 3 Unlock
