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Component: LO-ECH
Component Name: Engineering Change Management
Description: The production in line with the regulations of the American Food and Drugs Administration FDA for the production of drugs for human and animal use 'Good Manufactuing Practice' - GMP. Manufacturers and sellers that want to sell their products on the US market must comply with these regulations and be able to provide proof of compliance.
Key Concepts: Regulated production is a process in SAP's LO-ECH Engineering Change Management component that helps to ensure that all changes to production processes are properly documented and tracked. It helps to ensure that all changes are made in accordance with the company's policies and procedures. It also helps to ensure that any changes made are properly communicated to all stakeholders. How to use it: Regulated production can be used to track and document any changes made to production processes. This includes changes to the materials used, the equipment used, and the processes themselves. It also helps to ensure that any changes are properly communicated to all stakeholders. Tips & Tricks: When using regulated production, it is important to ensure that all changes are properly documented and tracked. This includes documenting the date of the change, who made the change, and what the change was. It is also important to ensure that any changes are properly communicated to all stakeholders. Related Information: For more information on regulated production, please refer to SAP's LO-ECH Engineering Change Management documentation. Additionally, there are many online resources available that provide more detailed information on how to use regulated production in SAP.