Category: QAD Practice News

As companies implement QAD EE and its .Net interface when they convert from other ERP systems or as they upgrade from previous versions of QAD’s ERP software, the power of browses continues to add value! Power users and IT teams who understand where QAD EE data resides can easily create browses which can be used on an ad hoc basis or linked to a menu and accessed by all users...

As Logan Consulting continues to work with clients to successfully implement ERP systems at client facilities, a detailed cutover plan needs to not only account for ERP related end user training and data conversion to prepare the ERP system for the go-live, it also needs to consider related equipment. In addition to data related tasks, it is critical to test the use of all equipment prior to cutover to confirm...

Logan Consulting will start a number of new ERP implementation projects in thee new year! For our new clients who do not have a well-defined SharePoint structure, Logan Consulting's SharePoint structure does an excellent job of supporting our ERP implementation projects. Logan Consulting utilizes Sharepoint extensively as part of our methodology, and it has become an integral tool to support our projects. In addition to the SharePoint lists for a...

As this is continual area of emphasis for ERP go-lives that we are involved in, we thought we would re-iterate the importance of this topic, written about back in 2014 as the importance of it has not diminished! The cutover to a new ERP system, or Go-Live, is often a difficult and stressful event for those involved. As the typical cutover weekend approaches and passes, teams often neglect the definition...

Having presented a session with a great client and attended other sessions, I view this conference as a success. Although we missed the personal interaction and side conversations with clients, vendors and QAD during the normal course of an in-person conference, the board did a good job of structuring and organizing this event. Logan Consulting appreciated being able to lead and participate in the following sessions: Success Story: GHSP Upgrade...

In the wake of the Covid-19 outbreak, manufacturers across the globe have made difficult decisions to keep up with the rapidly changing demands of the market and to mitigate unforeseen and often devastating risks to their businesses. Whether it be supply chain disruptions, factory shutdowns, or under- or over-production of inventory, almost all industries have felt the wide-reaching effects of the pandemic. As budgeting season rolls around, it is important...

For complex QAD Enterprise Applications projects, the importance of a concise and accurate Data Conversion Tracker managed in Microsoft Excel or SharePoint is critical to a successful cutover. During the last several weeks leading up to a Go-Live, management of the static, master, and dynamic data; along with the data ownership and status is important, as is the ability to view status metrics at any given time to view progress...

Years ago Logan Consulting started working with its clients on various requests from them to develop tighter integration with third partner logistics providers and warehouse partners (abbreviated 3PL, or sometimes TPL). This originally included very custom approaches to order processing within QAD and the added functionality to integrate with a TPL. Over the years, a common model has evolved leveraging standard QAD Enterprise Material Transfer (EMT) and EDI functionality to...

Many ERP implementations involve development as part of the project. Development in this context can mean any or all of the following: Development of new functionality to address a functional gap in the software Development of customer or supplier facing forms such as a Packing Slip, Shipper, Sales Order Acknowledgement, or Purchase Order Development of internal or customer facing labels Development of new reports, inquiries, or browses that present system...

Purpose The FDA outlines general principles that should be applied to the validation of medical device software or the validation of software used to design, develop, or manufacture medical devices. Scope The FDA outlines acceptable elements of software validation. However, these recommendations are not the extent of proper compliance. There are many other activities and tasks that must be completed in order to be compliant. It is each manufacturer’s responsibility...