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Digitization of the Regulatory Review

July 22, 2021 by Sara Bresee and Matt Lowe, MasterControl Inc.

The FDA’s roadmap to digitization and remote audits includes more modernized approaches to regulatory oversight.
COVID-19 has been dominating the attention of organizations focused on the development and regulation of medical products. The U.S. Food and Drug Administration (FDA) has largely been in the spotlight, and under enormous pressure. Much like most companies, the agency has needed to adapt on the fly and employ advanced technology to fulfill its core responsibilities—ensuring public health and safety.

Read the full article HERE.

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