Question: QUESTION 2 6 A marketing authorisation ( MA ) includes which of the following? a . Quality system b . In - Process controls c
QUESTION
A marketing authorisation MA includes which of the following?
a
Quality system
b
InProcess controls
c
Personnel requirements
d
Records
points
QUESTION
Which of the following is not true with respect to continuous improvement
a
Mainly small improvements less likely to require major capital investment
b
Makes changes that are generally easier to implement
c
Requires experts who have a range of quality tools at their disposal
d
The ideas come from the workers themselves
points
QUESTION
Poka yoke can assist in process development through
a
All of these
b
Eliminating rework
c
Reducing variability so products are consistent
d
Eliminating mistakes and errors in any process
points
QUESTION
Examine the following definition
A deficiency which has produced, or leads to a significant risk of producing either a product which is harmful to the human or veterinary patient
If you were auditing a pharmaceutical site and found such a defeciency, which classification would it be
major deficiency
minor deficiency
critical deficiency
none of the others
points
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 ins
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