This piece would be helpful if you want to provide your vendors, customers or 3PL/4PL partners a user Interface to record result on your behalf for the Inspection characteristics for example physical condition of goods and other product parameters. You can even ask them to upload quality related documents. They can record result without installing […]
Purpose: This blog will help to identify the Business Object and event to develop custom Workflow. Introduction In Standard SAP, we have very limited Standard Workflows. If the Business requirement is out of Standard Workflows, then we must built/ develop the custom workflows. To develop custom workflows, we must know the Business Object which is […]
1. Purpose: This blog explains the process of inspection lot generation for EWM inspection types, Result recording, Usage decision and limitations for EWM inspection types in S/4 HANA 1809. 2. Introduction: As discussed in earlier configuration doc, we must do relevant configuration for QM with EWM integration and, we must activate the inspection types for […]
Introduction: Configurable materials is used to define products that have different variants Also Read: What is SAP QM Certification? The usage of configurable materials Show clearly in some industries like Textile, carton. By using Configurable material you will have one material code with different specification for each sales order. Due that quality inspection of Configurable […]
Purpose: The purpose of blog to explains about purpose control indicators of result confirmation in MIC. Also Read: SAP QM Certification Preparation Guide Here we will discuss about control indicators Like Required charc Optional Charc After Acceptance After Rejection Required Charc: If inspection characteristic is must to record the results then we must choose “Required […]
Purpose: The Purpose of this blog to provide step by step procedure to auto update the Inspection results values to batch characteristics. Introduction: Most of PP/QM consultant get the requirement to update the QM inspection results to batch characteristics, especially when they work for Pharmaceutical projects. To Perform MQC, QM inspection results should be updated […]
Purpose: The Purpose of this blog to provide the information about how to get the changed the results values for Inspection characteristic for an inspection lot.This is one of the common business requirements to have report which shows Old value and new value when the user change results for Inspection characteristics from results recording. Also […]
This document will show you how to manage and store the quality certificate from the vendor. Certificate of Analysis plays an important role in the Pharmaceutical industry. COA ensures the GxP practices have been followed during the Production of the goods. In this scenario of procurement of goods from the Vendor, the vendor is expected […]
If materials have the same set of operations and signs of control, they could be assigned to one Inspection Plan. It’s OK, when the tolerance limits of a specific inspection characteristic are the same for each material – there is need neither for Dependent Characteristic Specifications in Inspection Plan nor its mixed loading. But when […]
The main purpose of this blog post is to explain how to create a status profile and how to configure the logic for an automatic status update. The status profile is required when the system status does not provide/has the required statuses to meet the requirement. Using a status profile we can create our own […]
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