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From July 1st, the way of submission of application and evaluation data will be adjusted.

According to China's accreditation, CNAS issued the notice on adjusting the application and evaluation of data submitted by laboratories and related institutions, inspection institutions, and from July 1, 2016, we adjusted the way of submission of application and assessment of inspection and testing institutions. The original text is as follows:





Notice on adjusting the way of submitting and evaluating information submitted by laboratories and related institutions and inspection bodies

 

Relevant institutions and assessors:

 

The new accreditation business management system of CNAS Laboratory Laboratory (hereinafter referred to as "business management system") has been launched by the Secretariat of the China National Accreditation Committee for conformity assessment (CNAS). In order to improve work efficiency, reduce management costs and enhance service effectiveness, after full discussion and argumentation, CNAS Secretariat has decided to adjust the way of submission of relevant organizations' applications and evaluation data. The following matters are hereby notified as follows:






I. scope of application

    

  1. The relevant institutions shall use the new "business management system" application for evaluation projects (such as preliminary assessment, expansion and re evaluation) to follow the notice.

  2. The assessor will use the new "business management system" evaluation items (such as preliminary assessment, supervision, expansion, re certification) to comply with this notice.

  3. The appraisal and approval of the new business management system has been carried out according to the original method.






Two. Approval of application information submitted

    

  1. The electronic materials submitted by the organization shall be authentic and traceable, otherwise they will be disposed of according to the rules of recognition.

  2. All information of the application should be submitted to the electronic version, but the main contents of the application form, Schedule 1, schedule 2-1, schedule 5, proof of the legal status of the laboratory, and the star of energy. Product classification Table and Energy Star detection methods and laboratory testing procedures, the corresponding list of inspectors should be submitted in addition to the electronic version of the paper version, the specific content is shown in Annex 1.






Three, on-site review information submitted

 

  1. The electronic materials submitted by the assessors should be authentic and traceable, otherwise they will be dealt with according to the rules of conduct of the assessors.

  2. The on-site assessment data should be submitted to the electronic version only in the first meeting at the end of the last meeting, but the contents of the assessment report, Schedule 1, schedule 2, schedule 3, Schedule 4, schedule 5, schedule 6, Annex 3, Annex 5, Annex 6, additional instructions, rectification reports, information review notifications, on-site judges' impartiality, confidentiality and self-discipline declarations, and the declaration of probity's probity and self-discipline shall be submitted in addition to the electronic version, and the paper should be submitted to the Appendix 2.





 

The above adjustments have been implemented since July 1, 2016.

 

 

I hereby inform you.



  

Secretariat of China National Accreditation Committee for conformity assessment

June 7, 2016



Annex 1

 

Schedule of submission of approved applications


Serial number

Table name

mode

Remarks

One

Application for approval



Two

Text of authorized application

Paper and electronics


Three

Schedule of approved applications



Four

Schedule 1: list of key laboratories

Paper and electronics


Three

Schedule 2-1: list of laboratory rights signatories

Paper and electronics


Four

Schedule 2-2: application form for authorized signatories

Electronics


Five

Schedule 3: laboratory staff list

Electronics


Six

Schedule 4-1: application for accreditation testing capability and instrumentation (including reference material / standard sample) configuration / verification

Electronics


Seven

Schedule 4-2: application for approval of "Energy Star" detection capability and instrumentation (including standard substance / standard sample) configuration / verification form

Electronics


Eight

Schedule 4-3: calibration and measurement capabilities and equipment / reference material configuration / verification forms for application for Accreditation

Electronics


Nine

Schedule 4-4: application for accreditation of forensic / forensic scientific institutions equipment / standard material configuration / verification form

Electronics


Ten

Schedule 4-5.1: reference measurement capacity and instrument configuration / verification form for application approval

Electronics


Eleven

Schedule 4-5.2: laboratory reference material (reference material) configuration / verification form (medical reference laboratory)

Electronics


Twelve

Schedule 4-6: table of criteria

Electronics


Thirteen

Schedule 5-1: laboratory proficiency test / measurement review list

Paper and electronics


Fourteen

Schedule 5-2: laboratories participating in the inter laboratory comparison list

Paper and electronics


Fifteen

Schedule 6: verification form of quality management system (when completed for initial application)

Electronics


Sixteen

Schedule 7: laboratory scope of English proficiency (to be published when attachments to English certificates)

Electronics


Seventeen

Documents and materials submitted with the application form



Eighteen

The certification document of the legal status of the laboratory, including the business license of the legal person, the authorized document of the legal person or legal person representative (non independent legal laboratory), if there is no change, only provided when the initial application is made.

Paper and electronics


Nineteen

Effective quality manuals and procedures for Laboratories

Electronics


Twenty

The laboratory conducted the latest complete internal audit and management review information (submitted at the initial application).

Electronics


 

Twenty-one

Laboratory plan

Electronics


Twenty-two

Verification of the current validity of the standards / methods applied for Accreditation (submitted verification report)

Electronics


Twenty-three

Non standard method and confirmation record (proof material)

Electronics


Twenty-four

Typical project inspection report / calibration (reference measurement) Certificate / appraisal document and its uncertainty evaluation report

Electronics


Twenty-five

Energy star product catalog

Paper and electronics


Twenty-six

List of "Energy Star" detection methods, laboratory testing procedures, and testing personnel correspondence

Paper and electronics


Twenty-seven

Copy of application fee remittance document

Electronics


 


 

 

Annex 2

 

Detailed form of information submitted by assessors

 


Serial number

Table name

mode

Remarks

One

Review Report



Two

Main body of accreditation report

Paper and electronics


Three

Schedule of assessment report



Four

Schedule 1: list of key laboratories

Paper and electronics


Five

Schedule 2-1: recommended authorized laboratory authorized signatories (Chinese and English)

Paper and electronics


Six

Schedule 3-1: recommended laboratory capacity for testing (Chinese and English)

Paper and electronics


Seven

Schedule 3-2: recommended approval of "Energy Star" detection capability range (Chinese and English)

Paper and electronics


Eight

Schedule 3-3: list of recommended laboratory criteria (Chinese and English)

Paper and electronics


Nine

Schedule 4: "recommended calibration and measurement capabilities" (Chinese and English)

Paper and electronics


Ten

Schedule 5: recommended recognised judicial expertise / capacity of forensic science institutions (Chinese and English)

Paper and electronics


Eleven

Schedule 6: recommended reference range of measurement capacity (in Chinese and English)

Paper and electronics


Twelve

Annex of evaluation report



Thirteen

Annex 1-1: "laboratory site review checklist" (including application description verification form)

Electronics


Fourteen

Appendix 1-2: judicial review / verification form of forensic science field review (including application note verification form).

Electronics


Fifteen

Annex 2: record of accreditation of laboratory authorized signatories.

Electronics


Sixteen

Annex 3-1: "field test record form for testing / calibration / identification laboratory"

Paper and electronics


Seventeen

Annex 3-2: "medical reference measurement laboratory field test record form"

Paper and electronics


Eighteen

Annex 4: laboratory proficiency verification checklist.

Electronics


Nineteen

Annex 5: "laboratory nonconformance / observation record form"

Paper and electronics


Twenty

Annex 6: "acceptance of laboratory rectification"

Paper and electronics


Twenty-one

Annex 7: recommendations of the review team for follow-up supervision and evaluation.

Electronics


Twenty-two

Additional description

Paper and electronics


Twenty-three

Review and rectification report



Twenty-four

Review and rectification report

Paper and electronics


Twenty-five

Other review materials



Twenty-six

Information review notice

Electronic or paper quality

It is not recommended for on-site review, no approval, confirmation of paper examination, paper and electronic, and other cases only electronic.

Twenty-seven

Review schedule

Electronics


Twenty-eight

Fair, confidentiality and self-discipline statement of on-site assessors

Paper and electronics


Twenty-nine

Declaration of integrity and self-discipline of conformity assessment bodies

Paper and electronics


Thirty

First and last meeting check-in form

Paper quality


Thirty-one

Summary sheet

Electronics


Thirty-two

Notice of normative review of application for approval (if any)

Electronics


 



(source: speed up to ISO9001)


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