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Voice Assistants have proved their efficiency in facilitating R&D documentation, allowing effortless real-time data capture and access at the bench.

But if documenting is essential in R&D for protocols optimization and troubleshooting, it is a mandatory pain for cGMP-regulated work. Can voice assistants streamline cGMP documentation and make the process seamless and handsfree while supporting ALCOA+ principles?

Date: 24 November, 2020
 Time: xxxxx

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