Validation and compliance made easy
At this year’s P-MEC 2018, B&R will be presenting modular and flexible hardware and software solutions for pharmaceutical machines and factories. Visit B&R stall in Hall 10, Stall 10.A29 at India Expo Centre, Noida, Delhi from December 12-14, 2018 to witness smart manufacturing solutions for greenfield and brownfield as well as ensure compliance to 21 CFR Part 11. Another highlight would be B&R's revolutionary mapp technology, which accelerates software development by an average of 67%.
Achieving operational excellence
B&R will showcase various solutions for smart manufacturing enabling higher productivity, OEE and RoI. With ACOPOS P3, machine builders not only reduce cabinet space but also conserve energy and save costs. Hypervisor allows Windows or Linux to run alongside B&R's own real-time operating system, making it possible to combine a controller and HMI PC in one device. Pharmaceutical factories look at a seamless vertical and horizontal connectivity, which is satisfied by the vendor independent, secure OPC UA.
Applications in compliance with 21 CFR Part 11
Pharmaceutical companies need the ability to log operations performed by users seamlessly without risk of tampering. B&R's mapp Technology provides quick and easy way to implement and customize audit trails. System manufacturers and end users benefit from maximum security without having to implement organizational measures. mapp Report helps to automatically generate PDF reports based on any machine data, with a possibility of customization, layout and design. With mapp Database, it is possible to archive data directly from field level to a database, regardless of whether that database is located on site or in the cloud. This drastically simplifies the management of large volumes of data. With B&R solutions, machine builders achieve accelerated development and reduced investment risk for applications subject to 21 CFR Part 11 requirements.