17025

How To Get ISO 17025 Certification In Chennai

with No Comment

Qualitcert is a catalyst for business and process excellence, your business and process excellence is guaranteed through ISO certification in Chennai with Qualitcert  

Up your business, talk to our Qualitcert masters who are available for you to coach and on how to get your business and process certified with ISO 9001, ISO 14001, ISO 45001,ISO 22000,ISO 27001,ISO 20000-1 and HACCP.

How get your lab accredited with ISO 17025  through Qualitcert in Chennai ?

ISO 17025 general requirements for the competence of testing and calibration laboratories, every lab in Chennai must blend the standard requirements with the internal process to deliver the test results with accuracy and with impartiality. By acquiring this international standard, lab can strongly brand as technically competent. In many cases, suppliers and regulatory bodies will not entertain test or calibration results from a lab that is not accredited through accredited registrar. With Qualitcert your ISO 17025 accreditation is guaranteed.

This standard was framed and published by international organization for standardization in the year 1999.laboratories use ISO 17025 to implement a quality system driven to improve their ability to consistently produce accurate results with impartiality. The standard has undergone changes thrice and released in 1999, 2005 and latest version is ISO 17025 .

The key press was on the responsibilities of senior management, explicit requirements for continual improvement of the management system and communication with the customer. It modeled ISO 9001.The 2005 version of the standard has a simple structure with 5 elements blended; Normative references, Terms and definitions, Management requirements and Technical requirements. Management requirements mainly pushed to focus on quality, management system within the laboratory. Technical requirements include items that determine the accuracy of the tests and calibrations performed in the laboratory.

The new version of ISO 17025 has little more elements added to the structure, based on annexure SL, in total we have now 10clauses, Scope, Normative References, Terms and Definitions, General Requirements, Structural Requirements, Resource Requirements, Process Requirements, and Management System Requirements.

Why ISO 17025 ?

ISO 17025 is the unique and most sought after ISO standard for calibration and testing laboratories across the globe. ISO 17025 accredited laboratory’s have demonstrated that they are technically competent and able to produce the accurate test results and calibration data.

Laboratory that are accredited with ISO 17025 are able to shape up few key factors along with the accurate test result and calibration data

  1. Technical competence of staff
  2. Traceability
  3. Maintenance of test equipment
  4. Quality assurance of test and calibration data
  5. Validity and appropriateness of test methods
  6. Quality of testing environment and sampling

Why ISO 17025 ?How are customers benefited ?

ISO 17025 accreditation helps you pick up the right laboratory that has a technically competent staff and system. Customers searching for an ISO 17025 accredited entity can reach us at www.Qualitcert.com or write to us at [email protected] or call us on 9686433300.

Experts here at Qualitcert will handhold you throughout your accreditation process.

Structure of ISO 17025  clause 4, 5 and 6

Clause 4
What General Requirements
Objective Manage – Impartiality & confidentiality
Who Management + All staffs + External parties(if any)
Key Notes Impartiality :

  1. Identify potential risk associated to impartiality (Test Results).
  2. Include the risks arising from the LAB associated personnel, external party (customer – bribe or any material), Management.
  3. Have a mitigation plan for the same.
  4. Have an agreement signed (Unbiased Agreement).
  5. Have a unbiased team ( independent from the lab process).

Confidentiality :

  1. Customer should be informed in writing, if taking any information (Test Result or could be any data) to the public.
  2. All the associated personnel should sign a confidentiality declaration.
To Do List (Only Example) Documents :
Risk Assessment procedureRecords :
Risk register
Impartiality declaration
Confidentiality declaration
Risk Mitigation plan
Clause 6
What Resource Requirements
Objective Have a strong and competent resource
Who Management + All staffs + External parties(if any)
Key Notes
  1. Appoint the LAB supervisor (or LAB manager if) to monitor the personnel.
  2. Identify training need for the personnel.
  3. Have clean sophisticated environment to carry out the testing process.
  4. Have the right calibrated equipment to carry out the tests.
  5. Have unique part/ serial number track back the insatiable results.
  6. Have solid control over the purchasing of equipment & subcontracting the service.
To Do List (Only Example) Documents :
Training Procedure
Procedure to track up the uncertain of test results
Job description of all personnelRecords :
Risk register
Training Plan
Training feedback form
Purchase order

Documents required for ISO Registration Process in Chennai

When applying for an ISO Certification, will need to submit the following documents:

  1. Certificate of Incorporation
  2. MSME certificate
  3. GST certificate
  4. Additional local legal document
  5. Sale Invoice
  6. Purchase order

Along with the above list, we need to furnish additional supporting documents and same can be developed during ISO Consultation – Mandatory procedures and post Audit – Audit report.

How to get ISO 17025:2017 certification in Chennai – Consultants in Chennai ?

Our masters have more than 10 plus years of global experience, with hands-on experience in the field of ISO certification, assessment and training.

With Qualicert your Business and process excellence is guaranteed.

Reach us at : [email protected]

Talk to us :  9686433300

17025

How To Get ISO 17025 Certification In Hyderabad

with No Comment
ISO 17025 – Lab management system

Qualitcert is a catalyst for business and process excellence, your business and process excellence is guaranteed through ISO certification with Qulaitcert

Up your business, talk to our Qualitcert masters who are available for you to coach and on how to get your business and process certified with ISO 9001, ISO 14001, ISO 45001,ISO 22000,ISO 27001,ISO 20000 and HACCP.

ISO 17025 general requirements for the competence of testing and calibration laboratories, every lab in Hyderabad must blend the standard requirements with the internal process to deliver the test results with accuracy and with impartiality. By acquiring this international standard, lab can strongly brand as technically competent. In many cases, suppliers and regulatory bodies will not entertain test or calibration results from a lab that is not accredited through accredited registrar. With Qualitcert your ISO 17025 accreditation is guaranteed.
This standard was framed and published by international organization for standardization in the year 1999.laboratories use ISO 17025 to implement a quality system driven to improve their ability to consistently produce accurate results with impartiality. The standard has undergone changes thrice and released in 1999, 2005 and latest version is ISO 17025.

ISO 17025
Key Items Description
ISO 17025 Lab Management System
Year Published 2017
Objective
  1. Frame up a strong system ( Document what you do and take action)
  2. Keep the process impartial
  3. Keep the data confidential
  4. Keep the customer happy

Structure of ISO 17025

Clauses What
Clause 1 Scope
Clause 2 Normative Reference
Clause 3 Terms & Definitions
Clause 4 General Requirements
Clause 5 Structural Requirements
Clause 6 Resource Requirements
Clause 7 Process Requirements
Clause 8 Management Requirements
Clause 4
What General Requirements
Objective Manage – Impartiality & confidentiality
Who Management + All staffs + External parties(if any)
Key Notes Impartiality :

  1. Identify potential risk associated to impartiality (Test Results).
  2. Include the risks arising from the LAB associated personnel, external party (customer – bribe or any material), Management.
  3. Have a mitigation plan for the same.
  4. Have an agreement signed (Unbiased Agreement).
  5. Have a unbiased team ( independent from the lab process).

Confidentiality :

  1. Customer should be informed in writing, if taking any information (Test Result or could be any data) to the public.
  2. All the associated personnel should sign a confidentiality declaration.
To Do List (Only Example) Documents :
Risk Assessment procedureRecords :
Risk register
Impartiality declaration
Confidentiality declaration
Risk Mitigation plan
Clause 5
Key Items Description
What Structural Requirements
Objective LAB structure – Define and document all want
Who Management
Key Notes
  1. Identify right leader to carry forward the standard
  2. List all the legal and statutory requirements
  3. Have the organization chart framed
  4. Frame up the communication hierarchy (internal and External)
  5. Have the LAB policy framed
  6. List all the LAB activities ( include if any subcontracted)
To Do List (Only Example) Documents :
Job description of leader – ISO
Procedure for in identifying the legal & Statutory requirementsRecords :
Org chart
Communication hierarchy chart
Legal and statutory register
Activity List -LAB
Clause 6
Key Items Description
What Resource Requirements
Objective Have a strong and competent resource
Who Purchase + HR + Training
Key Notes
  1. Appoint the LAB supervisor (or LAB manager if) to monitor the personnel
  2. Identify training need for the personnel
  3. Have clean sophisticated environment to carry out the testing process
  4. Frame up the communication hierarchy (internal and External)
  5. Have the right calibrated equipment to carry out the tests
  6. Have unique part/ serial number track back the insatiable results
  7. Have solid control over the purchasing of equipment & subcontracting the service
To Do List (Only Example) Documents :
Training Procedure
Procedure to track up the uncertain of test results
Job description of all personnelRecords :
Org chart
Training Plan
Training feedback form
Purchase order
Clause 7
Key Items Description
What Process Requirements
Objective Have a strong sampling, test method(s) , validation , verification , reporting and information management system.
Who LAB Manager
Key Notes
  1. Define a contract / tendering procedure
  2. Identify training need for the personnel
  3. Identify the right sampling, testing and calibration methods and document the same
  4. Frame up the right reporting plan and also managing the technical record
  5. Frame up a customer complaint handling procedure
  6. Frame up a procedure to handle nonconformity of test work
  7. Implement information security polices to protect the data
To Do List (Only Example) Documents :
Contract/Tender Procedure
Procedure for sampling, Test and Validation
Customer complaint handling procedure
Information security policiesRecords :
Contract review
Results report
Customer complaint form
Clause 8
Key Items Description
What Management System Requirements
Objective Have a procedure to control documents, records, internal audit and corrective action
Who Management + LAB Manager + All staffs
Key Notes
  1. Frame up procedure to handle documents and records
  2. Perform internal Audit
  3. Perform Management Review Meeting
  4. Take corrective action
  5. Risk management ( blend with clause 4 – impartiality )
To Do List (Only Example) Documents :
Control of document procedure
Control of records procedure
Procedure to perform internal audit
Information security policiesRecords :
Internal audit calendar
Risk register
Minutes of meeting
Auditable Clauses
Clauses What
Clause 4 General Requirements​
Clause 5 Structural Requirements​
Clause 6 Resource Requirements​
Clause 7 Process Requirements
Clause 8 Management Requirements

Why ISO 17025 ?

ISO 17025 is the unique and most sought after ISO standard for calibration and testing laboratories across the globe. ISO 17025 accredited laboratory’s have demonstrated that they are technically competent and able to produce the accurate test results and calibration data.

Laboratory that are accredited with ISO 17025 are able to shape up few key factors along with the accurate test result and calibration data

  1. Technical competence of staff
  2. Traceability
  3. Maintenance of test equipment
  4. Quality assurance of test and calibration data
  5. Validity and appropriateness of test methods
  6. Quality of testing environment and sampling

How to get ISO 17025 certification ?

Our masters have more than 10 plus years of global experience, with hands-on experience in the field of ISO certification in Hyderabad, assessment and training.

With Qualitcert your Business and process excellence is guaranteed.

Reach us at :[email protected]

Talk to us :  9686433300

17025

How To Get ISO 17025 Certification In Bangalore

with No Comment

Qualitcert is a catalyst for business and process excellence, your business and process excellence is guaranteed through ISO certification in Bangalore with Qualitcert

Up your business, talk to our Qualitcert masters who are available for you to coach and on how to get your business and process certified with ISO 9001, ISO 14001, ISO 45001,ISO 22000,ISO 27001,ISO 20000 and HACCP.

How get your lab accredited with ISO 17025  through Qualitcert ?

ISO 17025 general requirements for the competence of testing and calibration laboratories, every lab in Bangalore must blend the standard requirements with the internal process to deliver the test results with accuracy and with impartiality. By acquiring this international standard, lab can strongly brand as technically competent. In many cases, suppliers and regulatory bodies will not entertain test or calibration results from a lab that is not accredited through accredited registrar. With Qualitcert your ISO 17025 accreditation is guaranteed.

This standard was framed and published by international organization for standardization in the year 1999.laboratories use ISO 17025 to implement a quality system driven to improve their ability to consistently produce accurate results with impartiality. The standard has undergone changes thrice and released in 1999, 2005 and latest version is ISO 17025.

The key press was on the responsibilities of senior management, explicit requirements for continual improvement of the management system and communication with the customer. It modeled ISO 9001.The 2005 version of the standard has a simple structure with 5 elements blended; Normative references, Terms and definitions, Management requirements and Technical requirements. Management requirements mainly pushed to focus on quality, management system within the laboratory. Technical requirements include items that determine the accuracy of the tests and calibrations performed in the laboratory.

The new version of ISO 17025  has little more elements added to the structure, based on annexure SL, in total we have now 10clauses, Scope, Normative References, Terms and Definitions, General Requirements, Structural Requirements, Resource Requirements, Process Requirements, and Management System Requirements.

Why ISO 17025 ?

ISO 17025 is the unique and most sought after ISO standard for calibration and testing laboratories across the globe. ISO 17025 accredited laboratory’s have demonstrated that they are technically competent and able to produce the accurate test results and calibration data.

Laboratory that are accredited with ISO 17025 are able to shape up few key factors along with the accurate test result and calibration data

  1. Technical competence of staff
  2. Traceability
  3. Maintenance of test equipment
  4. Quality assurance of test and calibration data
  5. Validity and appropriateness of test methods
  6. Quality of testing environment and sampling

How are customers benefited ?

ISO 17025 accreditation helps you pick up the right laboratory that has a technically competent staff and system. Customers searching for an ISO 17025 accredited entity can reach us at www.Qualitcert.com or write to us at  [email protected] or call us on 9686433300.

Experts here at Qualitcert will handhold you throughout your accreditation process.

Clause 4
Key Items Description
What General Requirements
Objective Manage – Impartiality & confidentiality
Who Management + All staffs + External parties (if any)
Key Notes Impartiality :

  1. Identify potential risk associated to impartiality (Test Results)
  2. Include the risks arising from the LAB associated personnel, external party (customer – bribe or any material), Management.
  3. Have a mitigation plan for the same.
  4. Have an agreement signed (Unbiased Agreement).
  5. Have a unbiased team ( independent from the lab process)

Confidentiality :

  1. Customer should be informed in writing, if taking any information (Test Result or could be any data) to the public.
  2. All the associated personnel should sign a confidentiality declaration.
To Do List (Only Example) Documents :
Risk Assessment procedure

Records :
Risk register
Impartiality declaration
Confidentiality declaration
Risk Mitigation plan
Clause 5
Key Items Description
What Structural Requirements
Objective LAB structure – Define and document all want
Who Management
Key Notes
  1. Identify right leader to carry forward the standard
  2. List all the legal and statutory requirements
  3. Have the organization chart framed
  4. Frame up the communication hierarchy (internal and External)
  5. Have the LAB policy framed
  6. List all the LAB activities ( include if any subcontracted)
To Do List (Only Example) Documents :
Job description of leader – ISO
Procedure for in identifying the legal & Statutory requirements
LAB Quality policy

Records :
Org chart
Communication hierarchy chart
Legal and statutory register
Activity List -LAB
Clause 6
Key Items Description
What Resource Requirements
Objective Have a strong and competent resource
Who Purchase + HR+ Training
Key Notes
  1. Appoint the LAB supervisor (or LAB manager if) to monitor the personnel
  2. Identify training need for the personnel
  3. Have clean sophisticated environment to carry out the testing process
  4. Have the right calibrated equipment to carry out the tests
  5. Have unique part/ serial number track back the insatiable results
  6. Have solid control over the purchasing of equipment & subcontracting the service
To Do List (Only Example) Documents :
Training Procedure
Procedure to track up the uncertain of test results
Job description of all personnel

Records :
Training Plan
Training feedback form
Purchase order

Documents required for ISO Registration Process

When applying for an ISO Certification, will need to submit the following documents:

  1. Certificate of Incorporation
  2. MSME certificate
  3. GST certificate
  4. Additional local legal document
  5. Sale Invoice
  6. Purchase order

Along with the above list, we need to furnish additional supporting documents and same can be developed during ISO Consultation – Mandatory procedures and post Audit – Audit report

How to get ISO 17025 certification ?

Our masters have more than 10 plus years of global experience, with hands-on experience in the field of ISO certification, assessment and training.

With Qualitcert your Business and process excellence is guaranteed.

Reach us at :  [email protected]

Talk to us :  9686433300