We all wonder what constitutes "Real World Evidence" to support our submissions to the FDA. May be you all know exactly what data to be collected for your submissions. Well not bad dialing into our free Webinar on 19th at 12 pm EDT and find out what else can be useful.
Towards a Real World Data - Informed Drug Development and Disease Control Programs | AAPS
Let us know if any aspects that we missed that may be useful to cover next on this topic from regulatory perspective. Hope you dial into the Webinar and reflect your thinking as a reply to this post.
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Raja Velagapudi Ph.D.
Excec. Director, Clinical Development
Sandoz Inc
Monmouth Junction NJ
[email protected]Disclaimer: Opinions expressed are solely my own and do not express the views or opinions of my employer.
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