Presently, in America , all the efforts are devoted to the development of Intelligent Manufacturing System (IMS) that can handle with all the activities related to the working floor.

FDA cGMP culture for 21st century is to encourage the adoption of advance new technologies and to adopt PAT (Process Analytical methodology). PAT is a system for designing , analyzing and controlling manufacturing through “ real time” measurements of critical quality attributes of raw and in-process materials and processes, with the goal of ensuring final product quality.

The fields of research in the USA focus on concept developments like Business to Manufacturing, Virtual Manufacturing, e-Manufacturing and Interoperability.

Netorus ERP/MES/FCS system presently includes all the activities related to the working floor. Indeed, Netorus ERP/MES/FCS system guarantees the validation success because:

- it implements the comprehensive guidance of the 21CFR parts 211, 210 for the good manufacturing practice of finished dosage, Q 7A for the good manufacturing practice of API and comply with part 11 for the computer system requirements.

- It provides your company, for the first time, with the controls to establish and maintain your production floor and your quality system in accordance to the regulation.