18 Jun 2021

Uncategorized
What is problem solving? What is problem solving? Problem solving is defined as the act of defining a problem, Identifying, prioritizing, and selecting alternatives for a solution and then implementing a solution. A problem – solving process is necessary for all business #management-systems. Why? Because #leadership wants to see continual improvement in their systems and identifying sol...
Read more

09 Jun 2021

Uncategorized
Quality! Why is it so important? Quality can be defined as the standard of something as measured against requirement; the degree of excellence of achieving the requirement. Each day we read through hundreds and thousands of reviews just so we can buy a quality product or service. Even individuals searching for an ISO 9001 training are looking to identify a training provider that will pro...
Read more

29 Mar 2021

ISO 9001, Uncategorized
Quality! Who does not want it. We read through hundreds and thousands of reviews each day just so we can buy a quality product or service. Even those searching for an ISO 9001 training are looking to identify a training provider that will provide a quality training. ISO 9001 is an international standard set by the International Organization for Standardization (ISO) that defines the fram...
Read more

28 Mar 2021

AS9100, Uncategorized
In the aerospace industry a small error in the supply chain can have disastrous consequences to the final product. AS9100 certification in the industry provides third party validation of the processes and organization has put in place to manage the quality of the product/service they deliver. It also helps to provide confidence to customers that they employ a process-based management sys...
Read more

27 Mar 2021

AS9100, Uncategorized
AS9110 Process Effectiveness Assessment Reports are used to identify the effectiveness of a process. PEAR was developed to allow audit personnel to systematically evaluate the effectiveness of a process as performed by the organization. It takes the inputs, outputs, actual steps of the process and recourses and controls in account. Turtle diagrams are often sued to depict PEARs. The P...
Read more

26 Mar 2021

Management System, Maritime, Uncategorized
Subchapter M ushered in a new era for the inland water companied within the US in the towing industry. The need for the regulation was driven by the many accidents that occurred on the inland waters of the US owing substandard vessels and incompetent personnel in use. As companies struggle to meet the requirements of the new regulation, those opting for the TSMS option seek documentation...
Read more

24 Mar 2021

ISO 9001, Training, Uncategorized
ISO 9001 training is a great starting point for those that do not have a good understanding of the ISO 9001 standard and are looking to implement it within their organization. The standard provides the framework for implementing a quality management system and defines requirements around the plan-do-check-act framework. ISO 9001 is also the basis for many other ISO standards such as ISO ...
Read more

23 Mar 2021

ISO 13485, Uncategorized
ISO 13485 sets the requirements for a quality management system for those organizations in the medical device industry. While there are many mandatory regulatory requirements issued by each country related to medical devices, ISO 13485 remains a voluntary standard. The need for certification to the standards stems either from a customer requirement or from a need to market to customers t...
Read more

22 Mar 2021

Uncategorized
We live in a world of super specialization. There seems to be a degree for every field and then subspecialty and further sub-sub specializations. It is not enough to be a banker anymore but there is a need for specialization in wealth management or mortgages of loans and so on. As the need for specializations and the associated training increases how does one determine the extent of ISO ...
Read more

20 Mar 2021

ISO 13485, MDSAP, Uncategorized
Quality is important in all industries but perhaps more so in the medical industry and for those organizations producing medical devices. Apart from ISO 13485 that defines the requirement for medical device quality management systems, medical device manufacturers have to also comply with the regulations of the country their devices are going to be used within. In an effort to streamline ...
Read more