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GENERAL QA/QC PROCEDURES FOR TESTING LABORATORIES (PART 1)

Total questions: 10

Worksheet time: 4mins

Name
Class
Date
1.

What is Laboratory Quality? (Multiple answers)

a)

Conformance to customer specification

b)

Able to achieve precision and accuracy required

c)

Zero non-conformity

d)

Accurate, reliable and traceable of test result

2.

WHAT IS LABORATORY QUALITY ASSURANCE (QA)? (Multiple answers)

a)

an ongoing, comprehensive program which analyzes every aspect of an entire operation/ processes

b)

determining a quality goal, deciding whether or not the goal has been achieved, and implementing corrective action if the goal has not been reached

c)

Insurance for laboratory

d)

written policies and procedures are established and followed to monitor and evaluate the ongoing and overall quality of the total testing process

3.

WHAT IS LABORATORY QUALITY CONTROL (QC)?

a)

Quality control personnel

b)

Methodologies / measures used to determine, monitor and verify the effectiveness of the quality assurance programme

c)

Quality control procedures

4.

Personnel competency verification and assessment is required prior authorized to perform specific test / task (Multiple answers):

a)

To ensure the accuracy achieved by the personnel

b)

To monitor the consistency of the personnel

c)

Ensure personnel attitude during test

d)

Personnel is able to demonstrate and conduct the test accordance to procedure

5.

Method verification is...

a)

verification, where the specified requirements are adequate for an intended use

b)

provision of objective evidence that a given item fulfils specified requirements

c)

The ability of a method to determine accurately and specifically the analyte of interest in the presence of other components in a sample matrix under the stated conditions of the test

d)

The ability of a method to measure only what it is intended to measure. To determine any interference affect the result

6.

Method validation is ...

a)

provision of objective evidence that a given item fulfils specified requirements

b)

The ability of a method to determine accurately and specifically the analyte of interest in the presence of other components in a sample matrix under the stated conditions of the test

c)

verification, where the specified requirements are adequate for an intended use

d)

The ability of a method to measure only what it is intended to measure. To determine any interference affect the result

7.

When normally we use the Certified Reference Material / Standard for? (Multiple answers)

a)

For calibration / intermediate checks

b)

As Quality Control sample (reference value) during testing

c)

For method verification and validation

8.

Purposes of audits? (Multiple answers)

a)

Check compliance with requirements

b)

Effectiveness of management system

c)

To initiate correction and corrective action

d)

Evaluate the needs for improvement

9.

PDCA means?

a)

Please; Do; Come; Again

b)

Plan; Do; Check; Act

c)

Plan; Do; Check; Again

d)

Plan; Do; Compromise; Action

10.

In PDCA Diagram, Do = Act?

a)

Yes. Do and Act both mean implement action

b)

No. Do means implementation; Act means correction and corrective action

c)

None of the above