Aug 302011
 

Many of the ISO standards are designed around the process approach to auditing and design of the management system and takes you away from clause based systems.

Organisations who introduce ISO 9001, AS9100, AS9120, AS9110 etc need to ensure their management systems are utilising the Plan Do Check Act definitions and steer away from clause based auditing and system design.  This is also relevant to organisations implementing other standards such as ISO 14001.

Within ISO 9000, the definition of a process is: A set of interrelated or interacting activities which transforms inputs into outputs.

Inputs to a process are generally outputs from other processes and a process has a start and an end defined by two limits and must be considered when defining your own processes.

Within ISO 9001 and AS9100, clause 4.1 requires organisations to (e) monitor, measure where applicable, and analyse these processes, and (f) implement actions necessary to achieve planned results and continual improvement of these processes.

The above clause is very important and is commonly overlooked by organisations and auditors.  Many organisations applying AS9100, AS9120 or AS9110 will be aware of the the new Process Effectiveness Assessment Report (PEAR) form which auditors shall begin to use during assessments.  These Reports are very important and will identify if your processes have been clearly defined and are suitably monitored and measured.  Further information on the PEAR shall be included within a separate blog.

Tools can be used to help organisations define their processes, these shall also be detailed within a separate blog but some example tools can be process flowcharts, SIPOCs and Turtle Diagrams.

Taking the above information, organisations need to ensure that their processes have been clearly defined with inputs and outputs and showing the interaction of these processes.  Measuring the effectiveness of the process is also vitally important and non-conformance’s shall be raised if these processes are found to be ineffective.

You can be in compliance with a clause of ISO 9001 or the Aerospace Standards but still be non-conforming if you are not monitoring and measuring a defined process and taking corrective actions against any areas which are outside of the defined requirements or targets.

A prime example of this could be late deliveries, if you have a process for delivering products within a defined time frame and you are late or outside of that requirement then a non-conformance’s should be raised internally and corrective actions taken.

Please note that this is a requirement of ISO 9001 not just the aerospace standards.  Review clause 4.1 carefully and consider your processes and how you are defining, monitoring and measuring those processes.

If you need to download some process tools or the PEAR form visit the IMS website.

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Jun 072011
 

last few spaces available for the ISO 9001 Lead Auditor course in Redditch available.

 

To book your space contact IMS on 01376 500068 or email info {at} imsworld(.)org

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Mar 212011
 

The United Kingdom Accreditation Service (UKAS) is the Sole Appointed National Accreditation Body within the United Kingdom.

On the 9th July 2008 the EU Parliament and the Council of the European Union adopted the EU Regulation 765/08 on Accreditation and Market Surveillance.

With effect from the 1st January 2010, the EU Regulation established a legal framework for the provision of accreditation services across Europe.  The Department for Business Innovation & Skills appointed the United Kingdom Accreditation Service (UKAS) as the UK’s NAB.

UKAS are signatories to the International Accreditation Forum (IAF), the European Co-operation on Accreditation (EA) and the International Laboratory Accreditation Co-operation (ILAC).

If you are responsible for ensuring your business is certified make sure the certification body you select is accredited by UKAS.  UKAS Accreditation provides assurance in the market as UKAS accredited certification bodies operate to recognised standards.  The accreditation process provides consumers with the confidence that the quality of the service they procure is of a consistently high standard.

Choosing a UKAS Accredited Certification and/or Inspection Body adds a number of benefits to your business which include:

  • de-risk your procurement by taking the guesswork out of choosing a certification body and by giving you the confidence that you will get the service that best fulfils your requirements;
  • win new business particularly since the use of accredited services is increasingly a stipulation of specifiers, most notably in the public sector;
  • facilitate access to international markets since UKAS accredited certificates are recognised throughout the world;
  • help you to identify best practice since your certification body is required to have appropriate knowledge of your business sector;
  • control costs with the help of knowledge transfer since accredited certification bodies can be a good source of impartial advice;
  • offer market differentiation and leadership by showing to others credible evidence of good practice;
  • demonstrate due diligence in the event of legal action;
  • reduce paperwork and increase efficiency by reducing the necessity to re-audit your business

IMS International LLP are accredited by UKAS (Certification Body number 078) for ISO 9001:2008, ISO 14001:2004, AS9100 Rev B, AS9120 and ISO 9001:2008 TickIT.

Reliance Technical Service Ltd are accredited by UKAS (Inspection Body number 0430) for ISO 17020 inspections.  Reliance are also a Notified Body (NB 2141) for the Safety of Toys for Europe.

Dongguan Testing Laboratory are accredted by CNAS (Testing Laboratory Number 3783) for the testing of toys to EN71 for the Safety of Toys.

For further information on the IMS group and the services we provide, visit our main website www.imsworld.org

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Dec 102010
 

The International Organisation for Standardisation (ISO) is giving users the opportunity to feedback on the use of the international Quality Management Standard; ISO 9001 and help shape future revisions.

ISO’s technical committee 176, subcommittee 2, completed its amendment to ISO 9001 in 2008 and its revision to ISO 9004 in 2009. Now it’s considering whether these revisions and related standards in the ISO 9000 family should be revised and what such revisions should consist of.

ISO requests that anyone who uses or will use ISO 9000 standards complete its ‘ISO 9000 User Survey’ and contributes their opinions on how the standards can be improved. The survey takes around 30 minutes to complete and will be open until January 2011.

Although the survey will take 30 minutes it will give you the chance to voice your opinions and concerns for future revisions of ISO 9001.  Many organisations feel that some areas could be more clearly defined or improved so now is the chance to hopefully bring those to light with the people who produce the standards.

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Nov 242010
 

The latest date for the ISO 9001:2008 IRCA Registered Lead Auditor Course has been set for the 7th-11th February 2011.  The course teaches you everything you need to know in order to attain your lead auditor status but will also provide you with the knowledge required to perform internal or supplier audits.

The course location has yet to be established but we will update you of this when it has been agreed.

If you would like to book a placement on the course or would like any further information please do not hesitate to contact IMS.

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Sep 042010
 

IMS International in Partnership with CMC International have spaces available for the next ISO 9001:2008 IRCA Lead Auditor Course to be held the week commencing 8th November 2010 at the Dunton Hills Golf Course in Brentwood, Essex.  The price of the course is £600 plus VAT and lasts for 5 days, all course literature is provided within the cost and lunch is provided.

The course is IRCA Registered and will allow all successful attendees to become approved Lead Auditors and perform internal audits or third party external audits.

If you are interested in attending the course please contact the IMS office on 013676 500068 or send an email to info {at} imsworld(.)org.

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Jun 122010
 

Not everyone is 100% clear on the certification process from initial application to the certificate being issued so we have developed this simple flowchart to detail this.  It also highlights what the auditor will be looking at during each of the stages (stage 1 and stage 2).

The same process will be followed should a currently certified client wish to add another site or standard such as ISO 14001 when they already have ISO 9001 in place.

If you require any specific or further information please do not hesitate to contact us.

ISO Certification Audit Process

ISO Certification Audit Process and what the Auditor will review during the stage 1 and stage 2 audit

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Jun 042010
 

The scope of certification is often overlooked by clients and it is very important that the scope reflects your activities.  The scope of certification needs to be unambiguous and consistent with your activities.

The scope of certification and audit is shown on the audit plans which is submitted a few weeks prior to the audit taking place, clients need to review this scope and ensure that no changes are required.   Unplanned scope changes cannot be amended during the audit and any changes need to be formally submitted to IMS prior to any activity.

A review is required of the requested changes to ensure that the current assigned auditor is competent to perform the audit against the amended scope, and that enough time has been allowed to complete the audit including the changes required.

If your current scope of certification is the “Refurbishment of Private Dwellings” and you now expand into “Demolition of Properties” then this area will need to be audited in order to bring it into your scope.  This process needs to be planned into the forthcoming audit and consideration needs to be taken for the auditor competence, no auditor will be allowed to arrive on the day of the audit and change the scope.

There will not generally be an issue bringing new activities into your scope and in most cases additional audit time will not be required.  However, auditors are not authorised to make that decision during the audit, therefore it is very important that you let the head office know prior to the audit that you wish to make a change to the scope.

Please ensure that when you receive the audit plans these are reviewed for content and times and the scope remains accurate.  Contact the head office as soon as possible to request a scope change, this must be received in writing.

If you have any questions regarding the above then please do not hesitate to contact us.

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Jun 032010
 

November 2008 marked the release of ISO 9001:2008 to replace ISO 9001:2000 and brought with it a number of minor amendments.

Whilst most client’s have already implemented the changes required to meet the new standard there still remains a number of organisations who need to make the changes in time for the deadline.

All organisations currently certified to ISO 9001:2000 have until the 14th November 2010 to complete the transition otherwise their certification will lapse and the certification process will need to start again.

There were not any major changes to the standard so transition should not be a timely or difficult task, however, client’s will need to read the new standard carefully as some of the changes or not immediately apparent.

If anyone is concerned that they may not be able to make the deadline please do not hesitate to contact IMS and we will aim to help you as much as possible.

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