If you are someone who is looking into getting an ISO 14001, then you may be wondering exactly why it is that you have to get this accreditation. First, you have to understand that ISO stands for the International Organisation of Standardisation. This is a series of standards that have been developed with a singular level of guidance for all companies to measure up to. The particular 14001 deals with the requirements that you will need to have in order to measure up to the environmental standards that have been set forth by the ISO.
While you do not necessarily have to get the ISO 14001 accreditation to operate your business, it is something you can do to prove to your clients and customers that you are doing your part to help out with the environment. However, you may be confused on how to go about getting this important accreditation, but it is not as difficult to attain as you might think, and most businesses should be able to get the certification within a year of the application. You should know that they will want to make sure that you have been following some form of environmental standards for at least three months prior to your application. To do this you can write an environmental review of your company's environmental impact as it is in its current operating state. You will then want to make sure that you provide this information when you send off your initial paperwork to begin the overall process.
In order to help prove that your company is doing its part to be environmentally aware you will have to go through an initial audit once the application has been filled out and filed. After the audit has been completed you will get a list of issues that the auditor feels you need to resolve before you can be certified for the ISO 14001. You will need to work on and correct these issues before the second audit is conducted, and they will give you a time period (usually three to six months) when they will return to check on your progress.
When the second audit occurs they will once again assess the overall business and then they will address the issues that were laid out in the previous audit. If everything goes well then your company will have proven that they are doing what they can to meet the standard set forth in ISO 14001, and they will then receive accreditation. However, this is not the end of the process. Even though you are now recognised as having environmentally conscious policies that are congruent with the international standards, you will have to go through periodic audits every three years to make sure that you are still operating correctly. Not only this, but every three months partial aspects of your company will be analysed to see that they are still working within the standards as well. As long as you remain within the compliance terms you will continue to receive your ISO 14001 certification.
Source: http://ezinearticles.com/
Saturday, October 23, 2010
Friday, October 22, 2010
How to Boost Exports Through Laboratory Accreditation?
Every businessman desires that he should be able to export maximum and that whatever he exports be readily acceptable to clients in the world market without any hassle. This is possible only if he exports quality products which have been tested by a reliable laboratory in his own country.
But the question remains as to how can we be sure that the results provided by a certain lab are really authentic? It is this requirement of authenticity that forces us to approach a lab that is accredited according to the requirements of international standard, ISO 17025.
For exporters, it is a big headache whether the product their clients are exporting comes up to the requirements of the international standard. Exporters might have also obtained valid certificate for the same, yet the importer would not necessarily have confidence that the laboratories' certificates obtained will be accepted. For his own satisfaction, he may require the product to be tested again. This creates difficulty, delay, and leads to wasteful extra costs.
The overseas importer on his part would be safe from all troubles at his end if he trusts the test certificates issued in the exporter's country which is the only sensible way left for both the parties if they use the services of accredited laboratories.
A National Accreditation Council (NAC) in any country ensures whether the laboratory is competent to undertake the tests; the equipment used was fit for the purpose; the testing methods were appropriate; the staff fulfilled the required standard of competence; appropriate records were kept; and much, much more!
ISO 17025 is an international standard that spells out general requirements for the competence of testing and calibration laboratories, which are 25 in number: 15 pertain to management, while 10 belong to technical side. The standard contains all such requirements that testing and calibration laboratories have to meet. This would be necessary if the laboratories wish to demonstrate that they operate a quality system, are technically competent and are able to generate technically valid results. Any laboratory that fulfils these requirements and confirmed by the NAC after due assessment, would be declared as an accredited laboratory.
It may be mentioned that before opting for accreditation, it would be worthwhile if a Gap Analysis of the lab is carried out. It's a one or two days' exercise that apprises the management of the lab as to where the lab stands at present and where it should be as far as international standard was concerned. The person conducting the Gap Analysis gets a fair idea as to how much efforts would be required to bring the lab up to an acceptable level so as to comply with the 25 requirements of ISO 17025.
Now, let's discuss these 25 requirements:
A. Management Requirements
1. Organization 2. Management system 3. Document control 4. Review of requests, tenders and contracts 5. Subcontracting of tests and calibrations 6. Purchasing services and supplies 7. Service to the customer 8. Complaints 9. Control of non-conforming testing and/or calibration work 10. Improvement 11. Corrective action 12. Preventive action 13. Control of records 14. Internal audits 15. Management reviews.
B. Technical Requirements
1. General 2. Personnel 3. Accommodation and environmental conditions 4. Test & calibration methods and method validation 5. Equipment 6. Measurement traceability 7. Sampling 8. Handling of test and calibration items 9. Assuring the quality of test & calibration results 10. Reporting the results.
The success of the accreditation program mainly depends on how successfully it is implemented and that depends upon the seriousness of the management i.e. how much committed the top management is! The whole process takes a period of six months. All the 25 requirements are addressed during this period, laying emphasis on the following main steps:
Main Steps
o An Introductory Lecture. To create awareness about laboratory accreditation among the lab staff, an introductory lecture is delivered and a brief description of all the clauses is given.
o Preparation of Quality System Documentation (QSD). The Quality Manual, Quality Procedures (both management and technical), work instructions and forms are to be prepared.
o Control of Non-conforming Testing and Calibration Work. The lab personnel are apprised as to which all actions would be necessary when a non-conforming test and calibration work is detected. The responsibility for the management of this non-conforming work would be designated.
o Corrective Action. Corrective action becomes necessary when anything wrong has happened. This is done through a Corrective Action Request (CAR) form. The implementation of such actions is followed through a Corrective Action Log (CAL) form which contains a list of these actions in an abbreviated form for reminding the management rep of the lab to follow the progress regarding such actions.
o Preventive Action. As opposed to the Corrective Action, Preventive Action is taken to preclude the possibility of any thing going wrong.
o Internal Audits. It's a proven fact that internal audits act as a lubricant for the quality management system of a lab. The more a lab is subjected to internal audits, the more its systems become stable. For conducting internal audits, a group of suitably selected personnel of the lab, say four to six in number, may be trained as internal auditors. The conduct of internal audits would be a planned activity and has to be taken seriously.
o Management reviews. Through Management Reviews, we control the entire process of quality management throughout the lab. The management review meetings must be attended by the head of the organization or the lab.
o Accommodation and Environmental Conditions. It means that accommodation and environmental conditions of the lab in which tests and calibrations are conducted should be appropriate.
o Methods. Appropriate methods would be used by the lab, preferably those methods which have been published in international, regional or national standards. Latest, valid edition of the standard would be used. The lab shall validate methods where necessary.
o Equipment. The equipment shall be operated by authorized personnel and would be calibrated before being placed into service. The test and calibration equipment shall be safeguarded from adjustments.
o Reporting the Results. The results shall be reported in a test report or calibration certificate and they will be reported accurately, clearly and unambiguously in accordance with the instructions in the test or calibration methods.
o Review of documents by Accreditation Body. Once a lab confirms that it is ready for accreditation to ISO 17025, it approaches one of the accreditation bodies for its assessment. The accreditation body asks for the documents of this lab for carrying out an independent check.
o Pre-assessment. The documents are checked by the accreditation body and sent back to the laboratory after check. The points / observations made by the accreditation body are resolved and accreditation body is informed by the lab. Then, the laboratory requests the accreditation body to conduct a final assessment of the lab.
o Final Assessment. The accreditation body conducts a final assessment of the lab. If the body finds that the lab conforms to all the 25 requirements of the standard (ISO 17025), it is recommended for final assessment and the lab is accredited.
Comparison with ISO 9001:2000 A question generally comes to the mind of the people: If a laboratory want to get accreditation as per ISO 17025, will it also have to get ISO 9001:2000 certification? The reply is a big NO! ISO 9001:2000 covers only management requirements whereas ISO 17025 covers both management as well as technical requirements. Hence, if a lab is ISO 17025, it needn't be certified to ISO 9001:2000 as management requirements are included in ISO 17025.
Benefits
By implementing ISO 17025, following benefits would accrue:-
o The processes of the lab would be qualified.
o The staff working in the lab would be properly trained and competent.
o An organised internal audit program will eliminate all the bugs in the working of the laboratory.
o The lab would be using validated methods.
o The responsibilities and authorities of the personnel in the lab will be clearly allocated.
o As proper sampling would be in vogue, there would be no need of resorting to repeated sampling which will save time, money and efforts.
o As all systems would be streamlined, customer complaints will be reduced and efficiency will increase.
o By carrying out proficiency testing, the clients will have more confidence in the results of the lab.
Conclusion. Accreditation of the laboratories is an inescapable requirement these days. It is a must for the authenticity of their results. By using the services of an accredited lab, there would be no need for a client to test the item again in his own country. If a lab is accredited, it means that it would be using calibrated equipment; its methods would be validated and the quality of tests and calibrations would be maintained. The results would be accurately reported and would be authentic. Regular annual assessments would keep the lab on track and its efficiency would be maintained. Last but not the least: the lab would join the elite group of the accredited laboratories of the world!
Source: http://ezinearticles.com/
But the question remains as to how can we be sure that the results provided by a certain lab are really authentic? It is this requirement of authenticity that forces us to approach a lab that is accredited according to the requirements of international standard, ISO 17025.
For exporters, it is a big headache whether the product their clients are exporting comes up to the requirements of the international standard. Exporters might have also obtained valid certificate for the same, yet the importer would not necessarily have confidence that the laboratories' certificates obtained will be accepted. For his own satisfaction, he may require the product to be tested again. This creates difficulty, delay, and leads to wasteful extra costs.
The overseas importer on his part would be safe from all troubles at his end if he trusts the test certificates issued in the exporter's country which is the only sensible way left for both the parties if they use the services of accredited laboratories.
A National Accreditation Council (NAC) in any country ensures whether the laboratory is competent to undertake the tests; the equipment used was fit for the purpose; the testing methods were appropriate; the staff fulfilled the required standard of competence; appropriate records were kept; and much, much more!
ISO 17025 is an international standard that spells out general requirements for the competence of testing and calibration laboratories, which are 25 in number: 15 pertain to management, while 10 belong to technical side. The standard contains all such requirements that testing and calibration laboratories have to meet. This would be necessary if the laboratories wish to demonstrate that they operate a quality system, are technically competent and are able to generate technically valid results. Any laboratory that fulfils these requirements and confirmed by the NAC after due assessment, would be declared as an accredited laboratory.
It may be mentioned that before opting for accreditation, it would be worthwhile if a Gap Analysis of the lab is carried out. It's a one or two days' exercise that apprises the management of the lab as to where the lab stands at present and where it should be as far as international standard was concerned. The person conducting the Gap Analysis gets a fair idea as to how much efforts would be required to bring the lab up to an acceptable level so as to comply with the 25 requirements of ISO 17025.
Now, let's discuss these 25 requirements:
A. Management Requirements
1. Organization 2. Management system 3. Document control 4. Review of requests, tenders and contracts 5. Subcontracting of tests and calibrations 6. Purchasing services and supplies 7. Service to the customer 8. Complaints 9. Control of non-conforming testing and/or calibration work 10. Improvement 11. Corrective action 12. Preventive action 13. Control of records 14. Internal audits 15. Management reviews.
B. Technical Requirements
1. General 2. Personnel 3. Accommodation and environmental conditions 4. Test & calibration methods and method validation 5. Equipment 6. Measurement traceability 7. Sampling 8. Handling of test and calibration items 9. Assuring the quality of test & calibration results 10. Reporting the results.
The success of the accreditation program mainly depends on how successfully it is implemented and that depends upon the seriousness of the management i.e. how much committed the top management is! The whole process takes a period of six months. All the 25 requirements are addressed during this period, laying emphasis on the following main steps:
Main Steps
o An Introductory Lecture. To create awareness about laboratory accreditation among the lab staff, an introductory lecture is delivered and a brief description of all the clauses is given.
o Preparation of Quality System Documentation (QSD). The Quality Manual, Quality Procedures (both management and technical), work instructions and forms are to be prepared.
o Control of Non-conforming Testing and Calibration Work. The lab personnel are apprised as to which all actions would be necessary when a non-conforming test and calibration work is detected. The responsibility for the management of this non-conforming work would be designated.
o Corrective Action. Corrective action becomes necessary when anything wrong has happened. This is done through a Corrective Action Request (CAR) form. The implementation of such actions is followed through a Corrective Action Log (CAL) form which contains a list of these actions in an abbreviated form for reminding the management rep of the lab to follow the progress regarding such actions.
o Preventive Action. As opposed to the Corrective Action, Preventive Action is taken to preclude the possibility of any thing going wrong.
o Internal Audits. It's a proven fact that internal audits act as a lubricant for the quality management system of a lab. The more a lab is subjected to internal audits, the more its systems become stable. For conducting internal audits, a group of suitably selected personnel of the lab, say four to six in number, may be trained as internal auditors. The conduct of internal audits would be a planned activity and has to be taken seriously.
o Management reviews. Through Management Reviews, we control the entire process of quality management throughout the lab. The management review meetings must be attended by the head of the organization or the lab.
o Accommodation and Environmental Conditions. It means that accommodation and environmental conditions of the lab in which tests and calibrations are conducted should be appropriate.
o Methods. Appropriate methods would be used by the lab, preferably those methods which have been published in international, regional or national standards. Latest, valid edition of the standard would be used. The lab shall validate methods where necessary.
o Equipment. The equipment shall be operated by authorized personnel and would be calibrated before being placed into service. The test and calibration equipment shall be safeguarded from adjustments.
o Reporting the Results. The results shall be reported in a test report or calibration certificate and they will be reported accurately, clearly and unambiguously in accordance with the instructions in the test or calibration methods.
o Review of documents by Accreditation Body. Once a lab confirms that it is ready for accreditation to ISO 17025, it approaches one of the accreditation bodies for its assessment. The accreditation body asks for the documents of this lab for carrying out an independent check.
o Pre-assessment. The documents are checked by the accreditation body and sent back to the laboratory after check. The points / observations made by the accreditation body are resolved and accreditation body is informed by the lab. Then, the laboratory requests the accreditation body to conduct a final assessment of the lab.
o Final Assessment. The accreditation body conducts a final assessment of the lab. If the body finds that the lab conforms to all the 25 requirements of the standard (ISO 17025), it is recommended for final assessment and the lab is accredited.
Comparison with ISO 9001:2000 A question generally comes to the mind of the people: If a laboratory want to get accreditation as per ISO 17025, will it also have to get ISO 9001:2000 certification? The reply is a big NO! ISO 9001:2000 covers only management requirements whereas ISO 17025 covers both management as well as technical requirements. Hence, if a lab is ISO 17025, it needn't be certified to ISO 9001:2000 as management requirements are included in ISO 17025.
Benefits
By implementing ISO 17025, following benefits would accrue:-
o The processes of the lab would be qualified.
o The staff working in the lab would be properly trained and competent.
o An organised internal audit program will eliminate all the bugs in the working of the laboratory.
o The lab would be using validated methods.
o The responsibilities and authorities of the personnel in the lab will be clearly allocated.
o As proper sampling would be in vogue, there would be no need of resorting to repeated sampling which will save time, money and efforts.
o As all systems would be streamlined, customer complaints will be reduced and efficiency will increase.
o By carrying out proficiency testing, the clients will have more confidence in the results of the lab.
Conclusion. Accreditation of the laboratories is an inescapable requirement these days. It is a must for the authenticity of their results. By using the services of an accredited lab, there would be no need for a client to test the item again in his own country. If a lab is accredited, it means that it would be using calibrated equipment; its methods would be validated and the quality of tests and calibrations would be maintained. The results would be accurately reported and would be authentic. Regular annual assessments would keep the lab on track and its efficiency would be maintained. Last but not the least: the lab would join the elite group of the accredited laboratories of the world!
Source: http://ezinearticles.com/
Thursday, October 21, 2010
How to Get an ISO 9001 Accreditation
The ISO 9001 accreditation is part of the International Organization for Standardization 9000 standards. They are awarded to businesses for quality. The 9001 is recognized worldwide as an award for a company's internal quality management or actions that the company takes to ensure the product or service they provide is of the highest quality. Customer satisfaction is a major factor in whether a company will be awarded an ISO 9001 accreditation.
There are many benefits for a company to have an ISO 9001 accreditation and the most important being that it gives a great impression of the business. If companies are planning to tender for a contract with a Local Authority for example, it can be one of the required criteria. Some of the other benefits include continuously detailed and quality driven running of your business, an improvement in customer satisfaction, improved business status, and an increase in staff motivation. A business can even integrate the ISO 9001 with other ISO standards such as those for health and safety, environmental and information security to further enhance the status of the company. The ISO standards all integrate together effortlessly so a business should have no problems maintaining ISO standards in all areas.
To get an ISO 9001 accreditation, your business will have to prepare and look for help and advice. You can check the ISO website for any advice on how to begin the process. You will need to find out everything you can before applying to see what you need to implement into your business. Find out as much as possible as this will ease your application process. Once you have decided to apply, a Lead Assessor will be appointed to you to help guide you through the whole process. Your lead assessor will be your first point of contact throughout and he or she should be able to answer any questions you have.
Stage one of the application process is the pre-audit assessment. This is where your lead assessor will visit your premises and make a report of everything you need to implement in order to gain your accreditation. After the visit you will be given a detailed report on all the necessary actions which need to be taken. You can then set a deadline for completing the required actions.
The second stage is the audit assessment. This will be set up for you by your lead assessor and an auditor will visit your premises and will notify you of any recommendations before leaving. If the auditor recommends that you be awarded the ISO 9001 accreditation, it will be confirmed shortly afterwards formally. You will then receive your ISO certification. However, the process does not end there. If you are awarded the certificate it is up to you to maintain the standards of quality that you have set. You will be continually assessed to ensure that your standards are maintained. You will still have the services of your lead assessor to help you to meet any requirements which are set down by the ISO 9001 standard.
Source: http://ezinearticles.com/
There are many benefits for a company to have an ISO 9001 accreditation and the most important being that it gives a great impression of the business. If companies are planning to tender for a contract with a Local Authority for example, it can be one of the required criteria. Some of the other benefits include continuously detailed and quality driven running of your business, an improvement in customer satisfaction, improved business status, and an increase in staff motivation. A business can even integrate the ISO 9001 with other ISO standards such as those for health and safety, environmental and information security to further enhance the status of the company. The ISO standards all integrate together effortlessly so a business should have no problems maintaining ISO standards in all areas.
To get an ISO 9001 accreditation, your business will have to prepare and look for help and advice. You can check the ISO website for any advice on how to begin the process. You will need to find out everything you can before applying to see what you need to implement into your business. Find out as much as possible as this will ease your application process. Once you have decided to apply, a Lead Assessor will be appointed to you to help guide you through the whole process. Your lead assessor will be your first point of contact throughout and he or she should be able to answer any questions you have.
Stage one of the application process is the pre-audit assessment. This is where your lead assessor will visit your premises and make a report of everything you need to implement in order to gain your accreditation. After the visit you will be given a detailed report on all the necessary actions which need to be taken. You can then set a deadline for completing the required actions.
The second stage is the audit assessment. This will be set up for you by your lead assessor and an auditor will visit your premises and will notify you of any recommendations before leaving. If the auditor recommends that you be awarded the ISO 9001 accreditation, it will be confirmed shortly afterwards formally. You will then receive your ISO certification. However, the process does not end there. If you are awarded the certificate it is up to you to maintain the standards of quality that you have set. You will be continually assessed to ensure that your standards are maintained. You will still have the services of your lead assessor to help you to meet any requirements which are set down by the ISO 9001 standard.
Source: http://ezinearticles.com/
Wednesday, October 20, 2010
Tuesday, October 19, 2010
Monday, October 18, 2010
Sunday, October 17, 2010
wise to change iso 9001 accreditation agency
• HealthBlawg: DNV senior execs speak with David Harlow about new ...
6 Nov 2008 ... By contrast, the ISO 9001 approach requires that there be some reliable process in place ... DNV standards change only if COPs or ISO 9001 standards change. ... Executive Vice President - Accreditation, and Becky Wise, ...
• Guidelines for Establishment of Accreditation of Health ...
and authorized agency accredits the quality system and competence of a ... wise approach is suggested, depending on the available resources. National ..... accreditation to ISO/IEC 17025, and not ISO 9001 certification. Obtaining .... development, the main concepts and core content will not change dramatically. ...
• Accrediting Agencies | Directory of Schools
Accrediting agencies are private educational associations of regional or ..... In 1998, ACCET became the only recognized accrediting agency to be certified as an ISO 9001-Quality ..... Arthur Wise, President 2010 Massachusetts Avenue, NW ... Master of Arts in Organizational Change. Keiser University eCampus ...
• Executive overview
certification body, the logo of the accreditation agency and the TickIT logo. ... It is wise, therefore, to read ISO. 9000:2000 before ISO 9001:2000. ... document, ISO 9001:2000. The greatest change is the new emphasis on processes ...
• The TickIT guide: using ISO 9001:2000 for software quality ...
anuary 2001 Issue 5.0 Board for Accreditation and Conformity Assessment (SWEDAC). ... It is wise, therefore, to read ISO 9000:2000 before ISO 9001:2000. ...
6 Nov 2008 ... By contrast, the ISO 9001 approach requires that there be some reliable process in place ... DNV standards change only if COPs or ISO 9001 standards change. ... Executive Vice President - Accreditation, and Becky Wise, ...
• Guidelines for Establishment of Accreditation of Health ...
and authorized agency accredits the quality system and competence of a ... wise approach is suggested, depending on the available resources. National ..... accreditation to ISO/IEC 17025, and not ISO 9001 certification. Obtaining .... development, the main concepts and core content will not change dramatically. ...
• Accrediting Agencies | Directory of Schools
Accrediting agencies are private educational associations of regional or ..... In 1998, ACCET became the only recognized accrediting agency to be certified as an ISO 9001-Quality ..... Arthur Wise, President 2010 Massachusetts Avenue, NW ... Master of Arts in Organizational Change. Keiser University eCampus ...
• Executive overview
certification body, the logo of the accreditation agency and the TickIT logo. ... It is wise, therefore, to read ISO. 9000:2000 before ISO 9001:2000. ... document, ISO 9001:2000. The greatest change is the new emphasis on processes ...
• The TickIT guide: using ISO 9001:2000 for software quality ...
anuary 2001 Issue 5.0 Board for Accreditation and Conformity Assessment (SWEDAC). ... It is wise, therefore, to read ISO 9000:2000 before ISO 9001:2000. ...
Saturday, October 16, 2010
iso 9001 accreditation
• ISO 9000 - Wikipedia, the free encyclopedia
Many countries have formed accreditation bodies to authorize certification bodies, which audit organizations applying for ISO 9001 compliance certification. ...
• ISO - International Organization for Standardization
International Organization for Standardization, responsible for the ISO 9000, ISO 14000, ISO 27000, ISO 22000 and other international management standards.
• ISO - Management standards - Choosing a certification body
When choosing a certification body to carry out ISO 9001:2000 (or ISO ...
• ISO 9001 Certification (ISO 9001:2008) : The British Assessment Bureau
Information on ISO 9001 certification, explaining the standard, ... We have over 40 years experience in the assessment industry and are UKAS accredited. ...
• The United Kingdom Accreditation Service
The United Kingdom Accreditation Service is the sole national accreditation body ... Accreditation of Pre-Shipment & Commodity Inspection to ISO/IEC 17020 ...
Many countries have formed accreditation bodies to authorize certification bodies, which audit organizations applying for ISO 9001 compliance certification. ...
• ISO - International Organization for Standardization
International Organization for Standardization, responsible for the ISO 9000, ISO 14000, ISO 27000, ISO 22000 and other international management standards.
• ISO - Management standards - Choosing a certification body
When choosing a certification body to carry out ISO 9001:2000 (or ISO ...
• ISO 9001 Certification (ISO 9001:2008) : The British Assessment Bureau
Information on ISO 9001 certification, explaining the standard, ... We have over 40 years experience in the assessment industry and are UKAS accredited. ...
• The United Kingdom Accreditation Service
The United Kingdom Accreditation Service is the sole national accreditation body ... Accreditation of Pre-Shipment & Commodity Inspection to ISO/IEC 17020 ...
Friday, October 15, 2010
change iso 9001 accreditation agency
• ISO certification - Aged Care Standards and Accreditation Agency
Aged Care - Standards and Accreditation Agency Ltd. Change text size .... Ltd has been accredited to the international quality management standard ISO 9001. ...
• ISO 9001 or ISO 14001 | LinkedIn Answers | LinkedIn
ISO 9001 or ISO 14001. In the context of ISO accreditation does anyone know ... IAC as your accreditation agency with BSI as your certification body because ...
• PLATINUM REGISTRATION : ISO 9001, Management System Registration ...
Without accreditation by an agency that belongs to IAF, there is no guarantee that a registrar's certificate represents conformity with ISO 9001. ...
• International Accreditation Agency
The International Accreditation Agency (IAA) is an independent and 'not-for-profit' ... ISO 9001 Quality Management; ISO 14001 Environmental Management ...
• NDUSTRY & GOVERNMENT RELATIONS COMMITTEE NAMSS Industry ...
The first change is in regard to "deeming authority." On July 15, ... three recognized hospital accrediting agencies: .... Methodology has been a staple of ISO 9001 surveys since ISO's inception in 1987. All areas ...
Aged Care - Standards and Accreditation Agency Ltd. Change text size .... Ltd has been accredited to the international quality management standard ISO 9001. ...
• ISO 9001 or ISO 14001 | LinkedIn Answers | LinkedIn
ISO 9001 or ISO 14001. In the context of ISO accreditation does anyone know ... IAC as your accreditation agency with BSI as your certification body because ...
• PLATINUM REGISTRATION : ISO 9001, Management System Registration ...
Without accreditation by an agency that belongs to IAF, there is no guarantee that a registrar's certificate represents conformity with ISO 9001. ...
• International Accreditation Agency
The International Accreditation Agency (IAA) is an independent and 'not-for-profit' ... ISO 9001 Quality Management; ISO 14001 Environmental Management ...
• NDUSTRY & GOVERNMENT RELATIONS COMMITTEE NAMSS Industry ...
The first change is in regard to "deeming authority." On July 15, ... three recognized hospital accrediting agencies: .... Methodology has been a staple of ISO 9001 surveys since ISO's inception in 1987. All areas ...
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