The documentation around clinical studies is large and diverse – and it all must adhere to GxP standards.

Learn how Heather Wolff, Vice President, Clinical Development Operations at Decibel Therapeutics, and her team of data managers, clinical operation experts, regulatory operations, medical writers, and biostats use Egnyte to streamline their compliance and data management processes.

And, to learn more about how Egnyte helps other life sciences companies store, share, and audit critical documentation around clinical trials, visit: Egnyte.com/solutions/life-sciences.

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