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B&R Acts As A Trusted Automation Partner For Leading Machine Builders
Express Pharma
|November 16-30, 2019
Jhankar Dutta, Managing Director – B&R Industrial Automation talks about how B&R is gearing up for CPHL 2019 and the various progressions the company has made in terms of innovation and digital upgradations
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Can you explain briefly about the company's portfolio?
B&R Industrial Automation, a member of the ABB group, is an innovative automation company with headquarters in Austria and offices all around the world. As a global leader in industrial automation, B&R combines state-of-the-art technology with advanced engineering to provide customers in virtually every industry with complete solutions for machine and factory automation, motion control, HMI and integrated safety technology. With Industrial IoT communication standards like OPC UA, POWERLINK and openSAFETY as well as the powerful Automation Studio software development environment, B&R is constantly redefining the future of automation engineering. The innovative spirit that keeps B&R at the forefront of industrial automation is driven by a commitment to simplifying processes and exceeding customer expectations.
We are global automation provider with groundbreaking motion control, machine operation and control solutions for pharmaceutical packaging. Our comprehensive portfolio fulfills all the requirements of a pharmaceutical packaging line – regardless of whether the product is in solid, liquid or powder form or whether it is packaged in blisters, paper, plastic, glass or metal. From blister packaging to fillers and cappers, from cartoning to case packers or palletizers, robotics, integrated machine vision and intelligent product transport – we provide the best automation solutions for pharmaceutical packaging machines and plants. We delivers products such as industrial PC, panels, transport systems, vision system, I/O systems, servo and stepper drives and motors, process control systems amongst others. All our hardware and software are fully compliant with FDA 21 CFR Part 11 regulations. In addition, we provide our customers an add-on package of technology libraries that support all FDA criteria for electronic records and signatures.
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