The Power of Real-World Data to Detect Adverse Events and Expedite FDA Postmarking Safety Commitments
Access Your Copy of the White Paper
To overcome the limitations inherent in traditional clinical trials, researchers increasingly are turning to real-world data (RWD) to provide a picture of a drug’s efficacy and safety. One example is our work with Ocular Therapeutix to satisfy FDA postmarketing safety requirements.
This white paper includes:
Why point-of-care EHR data is a game changer
Details on the Ocular Therapeutix ReSure Sealant Study
FDA and the use of real-world data
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