Take a Free Online ISO/IEC 17025:2017 Training Course

Gain the competence to plan the implementation of ISO/IEC 17025:2017 and develop a laboratory management system with this training course from UpWeld. Learn ISO/IEC 17025 today; find your ISO/IEC 17025 online course. Contact us for Certification ISOCert.In@Gmail.Com

“Uncertainty” is not a component of the Decision Rule.

TRUE

FALSE

All parts of a laboratory management may be documented either electronically or on paper

A. TRUE

B. FALSE

4.1 Organization:
What is the position title of the person who must have direct access to the highest level of management at which decisions are made on laboratory policies and resources?

A. Vice President

B. Technical Manager

C. Quality Manager

4.3 Document Control:

Document control means:

A. Ways to reduce paper

B. You give all documentation to your supervisor to maintain

C. Documents are identified, authorized, reviewed

It is not required to specify how a client conducts sampling

A. TRUE

B. FALSE

4.4 Review of requests, tenders, and contracts:
Requests, tenders, and contracts are reviewed for:

A. Client requirements and lab capability

B. Potential revenue

C. Spelling and grammar

Internal audits are only necessary for the years the laboratory is not assessed.

A. TRUE

B. FALSE

4.8 Complaints:
Records shall be maintained of all client complaints and of:

A. How angry the client is/was

B. The investigations and corrective actions were taken by the lab

C. How loud the client complained

A management system that conforms to ISO/IEC 17025:2017 includes consideration of risk assessment

A. TRUE

B. FALSE

10.

Which operations do the Technical Manager has the overall responsibility for to ensure the required quality of laboratory operations?

A. Quality

B. Technical

C. Both A and B

D. Neither A nor B

11.

Management review does not need the input of top management

A. TRUE

B. FALSE

12.

The following are the clauses in the 2017 version of the standard that contain requirements:

A. 2,3,5,7,9

B. 4,5,6,7,8

C. 2,3,4,5

D. Only clauses 6 and 7 have requirements

13.

Samples do not need to be tracked throughout the laboratory

A. TRUE

B. FALSE

14.

Which requirement specifically states the frequency of laboratory internal audits?

17025 does not specify a frequency for internal audits.

Clause 8.8 of ISO/IEC 17025:2017

Clause 8.7 of ISO/IEC 17025:2017

15.

If the method has been published in a standard, it does not need to be validated.

TRUE

FALSE

16.

What is the purpose of ISO/IEC 17025:2017?

It is to allow governments to accredit laboratories

It is to provide the tools that allow laboratories to produce consistent, technically valid results.

It is to allow laboratories to enter foreign markets

It is to force laboratories to use quality systems

17.

Uncertainties can be evaluated for non-numerical measurements.

TRUE

FALSE

18.

Why is the standard called ISO/IEC 17025:2017 and not ISO 17025:2017?

IEC paid money to the ISO to publish it

IEC participates with ISO in its development as part of CASCO

ISO is not the real copyright holder of ISO/IEC 17025

ILAC insisted that ISO allow the IEC name to appear in the standard

19.

Laboratories must include evaluation of uncertainties in statements of compliance

TRUE

FALSE

20.

The following feedback mechanisms are required in 17025:2017:

Publish all feedback on the website.

Record all complaints

Analyze all feedback

Ignore all feedback

21.

Once a non-conforming condition is observed, the laboratory should first:

Take action to control and correct it.

Find as many non-conformances as possible

Understand the process under review as it is understood by the person responsible for it

Allocate blame for the non-conformance

22.

Accreditation bodies conduct laboratory assessments:

Against ISO/IEC 17025 alone

Against ISO 9001 alone

Against ISO/IEC 17011 and ISO/IEC 17025

Against ISO/IEC 17025 and other accreditation requirements documents

23.

The object of the Decision Rule is

Determine the level of conformance of the object of testing/calibration to the specification

Relieve the client of responsibility in making compliance statements

Explain the lab result to a person not knowledgeable of the science

Protect the health, safety, and welfare of users of the object of testing/calibration

24.

Infernal audits are conducted to determine:

The conformance of laboratory operations to its own QMS and ISO/IEC 17025:2017

The conformance of laboratory operations with ISO 9001

The financial stability of the laboratory

The best suppliers of reference materials

25.

What does 17025:2017 require as considerations in metrological traceability to the SI?

Competence in calibration, unbroken chain of measurement, the contribution of uncertainty.

Systematic error, use of appropriate decision rule, use of OIML R 111 class weights

Self-declaration of competence, unbroken chain of measurement, specification of the measured.

CIPM MRA, Joint Declaration on Legal Metrology, unbroken chain of measurement

26.

What is the definition of the term “Impartiality”?

Absence of partiality

Lack of conflict of interest

Presence of objectivity

Freedom from bias, lack of prejudice, Neutrality

27.

A lab must meet all of the following requirements to demonstrate conformance to 17025:2017:

Demonstrate the consistent achievement of the requirements of 17025:2017 and assuring the quality of the laboratory results.

Meeting the requirements of Clauses 4 to 7 of 17025:2017.

Implement a management system in accordance with Options A or B of 17025:2017.

All of the above.

28.

ISO/IEC 17025:2017 contains the following types of requirements:

Management system and technical requirements

Management system and process requirements

Quality system and technical requirements

Leadership and management requirements

29.

When receiving a request for new work, the laboratory, according to 17025:2017, shall:

Determine its capability in doing the work.

Determine if it has the resources to do the work.

Confirm the method is fit for customer purposes.

All of the above.

30.

Documents and records acquired or created during testing and calibration work:

Are the property of the client of the lab.

Are to be retained for future reference by the accreditation body assessors.

Are to be sent to the accreditation body

Are to enable the repetition of the activity as close as possible to the original.

31.

The following are two options for a lab to implement a Management System:

Get certified to ISO 9001 – self-declare conformance to ISO/IEC 17025:2017

Get accredited to ISO/IEC 17025:2017 – self-declare conformance to ISO 9001

Self-declare conformance to 17025:2017 – self-declare conformance to ISO 9001

All of the above.

32.

Management review, according to ISO/IEC 17025:2017, requires examination of how many different issues/items overall:

33.

The concept metrological traceability in 17025:2017 applies to:

Calibration laboratories only.

Only physical measurement devices

Only measurement devices and certified reference materials and standards

All equipment contributes to the overall uncertainty of the measurement result.

34.

Traceability includes three components for each step in the traceability chain:

Uncertainty, calculation, documentation

Competence in calibration, uncertainty, traceability

Documentation, registration, reference to the SI

Competence in calibration, uncertainty, reference to the SI

ISO/IEC 17025 2017 Laboratory Accreditation Online Training Courses.

This is a Quiz Training Course for you to test your Knowledge of ISO IEC 17025. The ISO IEC 17025 2017 Training Course is also useful for laboratory clients, personnel of regulatory authorities and accreditation bodies who may use the knowledge gained in conforming or recognising the competency of testing and calibration laboratories.
Candidates for this course shall have attended awareness course on ISO / IEC 17025:2017

This ISO IEC 17025:2017 quiz Course presents multiple choice questions. You are to assume there is ONLY ONE CORRECT ANSWER. There are lots of questions.
Request for Certificte at ISOCert.in@Gmail.Com

Note: The ISO 17075 Internal Auditor certificate cost is 25 dollars. Certificate will provided by UpWeld.

If you want an IRCA/CQI Approved ISO 17025 Lead Auditor Certificate, then you need to attend our training seminar. The IRCA/CQI Approved Training and Certification Fees is 350 dollars.

3 thoughts on “Take a Free Online ISO IEC 17025 2017 Training Course”

anwar basha

June 25, 2022 at 7:37 pm

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- ANWAR BASHA SHAIK
  
  January 19, 2023 at 11:34 am
  
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- ILHAM ALAHMED
  
  March 8, 2023 at 1:40 pm
  
  I have completed Quiz successfully, please provide free certificate to the below mail

“Uncertainty” is not a component of the Decision Rule.

All parts of a laboratory management may be documented either electronically or on paper

4.1 Organization: What is the position title of the person who must have direct access to the highest level of management at which decisions are made on laboratory policies and resources?

4.3 Document Control:

Document control means:

It is not required to specify how a client conducts sampling

4.4 Review of requests, tenders, and contracts: Requests, tenders, and contracts are reviewed for:

Internal audits are only necessary for the years the laboratory is not assessed.

4.8 Complaints: Records shall be maintained of all client complaints and of:

A management system that conforms to ISO/IEC 17025:2017 includes consideration of risk assessment

Which operations do the Technical Manager has the overall responsibility for to ensure the required quality of laboratory operations?

Management review does not need the input of top management

The following are the clauses in the 2017 version of the standard that contain requirements:

Samples do not need to be tracked throughout the laboratory

Which requirement specifically states the frequency of laboratory internal audits?

If the method has been published in a standard, it does not need to be validated.

What is the purpose of ISO/IEC 17025:2017?

Uncertainties can be evaluated for non-numerical measurements.

Why is the standard called ISO/IEC 17025:2017 and not ISO 17025:2017?

Laboratories must include evaluation of uncertainties in statements of compliance

The following feedback mechanisms are required in 17025:2017:

Once a non-conforming condition is observed, the laboratory should first:

Accreditation bodies conduct laboratory assessments:

The object of the Decision Rule is

Infernal audits are conducted to determine:

What does 17025:2017 require as considerations in metrological traceability to the SI?

What is the definition of the term “Impartiality”?

A lab must meet all of the following requirements to demonstrate conformance to 17025:2017:

ISO/IEC 17025:2017 contains the following types of requirements:

When receiving a request for new work, the laboratory, according to 17025:2017, shall:

Documents and records acquired or created during testing and calibration work:

The following are two options for a lab to implement a Management System:

Management review, according to ISO/IEC 17025:2017, requires examination of how many different issues/items overall:

The concept metrological traceability in 17025:2017 applies to:

Traceability includes three components for each step in the traceability chain:

ISO/IEC 17025 2017 Laboratory Accreditation Online Training Courses.

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4.1 Organization:
What is the position title of the person who must have direct access to the highest level of management at which decisions are made on laboratory policies and resources?

4.4 Review of requests, tenders, and contracts:
Requests, tenders, and contracts are reviewed for:

4.8 Complaints:
Records shall be maintained of all client complaints and of: