CBG Inc. - Management System Professionals Support

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We created a new QMS Transition Workshop that will help you Better understand the ISO 9001:2015 Requirements Use this knowledge in the Staff and Internal Auditors training.   Plan and carry out 34 activities necessary to transfer the QMS to the new version of ISO 9001:2015  Our certificates are accepted by IRCA and RABQSA as evidence of continual professional development Check our website for the Workshop Outline Workshop length - 7 hours December 2015 price $189.00 includes: PDF certificate (0.7 CEU credits) QMS Transition Program Checklist ($79.00 value) Participants' Discount on selected ISO 9001:2015 Documents and Templates Slides and diagrams that can be used in auditor and stuff training Register now and save !

ISO as launched a survey for its Standards users on their level of understanding regarding its development process. ISO Management System Standards Survey  There is a lot of confusion over how Management System Standards are developed. Together we could make it better!

Here are some of Key Risks Wording for the 'Control of Personnel' Process: suboptimal personnel competence (including education, confirmed qualification, additional training, work experience);  inadequate system of motivation and stimulation;  lack of employee awareness ... And some of the Risk Treatment areas : correction of procedures for determining the necessary expertise;  correction of hiring procedure, including New employee orientations;  use of mentoring;  ... More Key Risks Wording and Risks Treatment areas in Risk Management in QMS Processes Quick Reference Guide Download the Risk Management in QMS Processes Sample Slides and use them in your ISO 9001:2015 internal auditor and personnel training. Other 9001:2015 documents and templates

ISO 9001:2015 requires to address the risks and opportunities in each process of the QMS. The principal questions of risk management are: Key Risks Wording and  Risk Treatment Areas    Here are some of Key Risks Wording for the ' Management Review ' Process: failure to achieve strategic goals;  failure to fulfill quality objectives;  slowdown in company activity performance indicator growth;  undesirable and not timely recognized QMS changes ... And some of the Risk Treatment areas : regularity and depth of Context of Organization analysis, communication and consideration for the decision-making;  analysis and review of QMS processes resources, including resources for monitoring and measuring;  improvement of planning methods ... More Key Risks Wording and Risks Treatment areas in Risk Management in QMS Processes Quick Reference Guide Other 9001:2015 documents and templates

Performing an audit is a major part of ISO 19011. New article by J.P. Russel ' Conducting Interview - Collecting and Verifying Information ' gives a quick review of ISO 19011 topics with practical tips: Conducting Interview - how the auditor should prepare for an interview and what info should be collected in advance; Interview environment - physical location, surrounding activities, the person to be interviewed; Interview guidance - how to start and finish the interview, what interview techniques to use in order to become efficient in achieving the results set; Pay attention to interfaces between processes in the management system Opportunities improvement - the questions the auditor should ask him(her)self to make sure opportunities for improvement are identified and addressed To help you out with Internal Audit process  - we've updated the Quality System Procedure Internal Audit according to the new ISO 9001:2015 Requirements More ISO 9001:2015 Documents...

A complete list of Risk Management Requirements Implementation in ISO 9001:2015 Clauses Objects of Control Subjects of Control Recommended Regulatory document (if provided in the Standard) Download Free Presentation also available in table format

Think through several options when making decisions. Think about consequences. Compile a clear risk list. Understand risk source. Give up neural networks and fuzzy logic for a while. Suggest a simple tool, such as  ‘risk level = probability * consequences’.            Suggest colleagues to estimate the first and second. The average result will be better than the result  from the application of artificial intelligence. Rank the risks by level and choose for risk treatment. Treat risks. Enhance desirable effects, prevent, or reduce, undesired effects. Make right decisions! Achieve an improvement! Enhance good practices. Describe positive experience in a documented procedure.  Risk Management Recommendations Examples of the most frequently used formulas     More  ISO 9001:2015 Transition tips on our site

ISO just published the long awaited New Version of ISO 9001! The Standard can be purchased in paper and electronic format . Experts from over 95 participating countries worked 3 years to bring the standard up to date with modern needs. If your Organization is ISO 9001 Certified (and over 1.1 million certificates were issued worldwide) you are granted a three-year transition period to migrate the QMS to the new edition of the standard. To facilitate the transition, we have prepared a set of ISO 9001:2015 Documents and Templates ISO 9001:2015 Overview. Presentation for Training ISO 9001:2015 Quality Manual Template Control of Documented Information in ISO 9001:2015 Clauses Comparative Analysis of ISO 9001:2015 vs. ISO 9001:2008 ISO 9001:2015 QMS Transition Program ...

The ISO community has provided information related to ISO 9001:2015 that may prove useful to organizations transitioning from the 2008 to the 2015 version. This information is free and available to the public at the ISO TC176/SC2 website:  ISO TC/176/SC2 Home Page 34 activities necessary to transfer the QMS to the new version of ISO 9001:2015 in out easy to use ISO 9001:2015 QMS Transition Program   Check out other ISO 9001:2015 documents and templates at http://c-bg.com/9001