This should be the title of the session

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?