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 30
According to ICH Q10, 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
2 points
QUESTION 31
Incidents must be formally reported by a QP
a.
False
b.
True
2 points
QUESTION 32
What is the minimum proving standard for a cleaning validation?
2 consecutive cleaning applications
3 consecutive cleaning applications
4 consecutive cleaning applications
5 consecutive cleaning applications
2 points
QUESTION 33
A clinical trial conducted according to a single protocol at more than one study centre is called a
a.
Multi-investigator study
b.
None of these
c.
Multi-country study
d.
Multi- centre study
2 points
QUESTION 34
For a Licensed Product, a widening of the specification would be regarded as a Major change
a.
False
b.
True
2 points
QUESTION 35
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
2 points
QUESTION 36
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
2 points
QUESTION 37
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
2 points
QUESTION 38
Which of these is used to test the transportation packaging and routes for pharmaceutical distribution?
transport verification
transport validation
transport qualification
transport monitoring
2 points
QUESTION 39
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.
Over-encapsulation
c.
Double dummy manufacture
d.
Capsulation
2 points
QUESTION 40
Records provide
a.
evidence of actions taken
b.
All of these
c.
demonstrate compliance with instructions
d.
raw data
2 points
QUESTION 41
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
2 points
QUESTION 42
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
2 points
QUESTION 43
Incidents non-conformities 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
2 points
QUESTION 44
Process equipment must be
a.
Stable
b.
Validated
c.
Randomly used
d.
Qualified
2 points
QUESTION 45
Continuous improvement activities can be applied to:-
a.
Process
b.
All of these
c.
Product
d.
Systems
2 points
QUESTION 46
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
2 points
QUESTION 47
The Fishbone diagram is also referred to as the
a.
Ishikawa diagram
b.
Kanri management diagram
c.
Effect diagram
d.
Jidoka diagram
2 points
QUESTION 48
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
2 points
QUESTION 49
The final report of an incident, non-conformity or deviation should be;
a.
All of these
b.
Clear, conci

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