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Digital Health Tools: What YOU Need to Know — Prepare now for the FDA’s Transformative Project
Want to attend the live webinar on Aug. 1? Click here to register.
The FDA is moving fast into development of digital health tools. The moves promise competitive advantage to the drug, biologics, device and combo products makers who position themselves to take advantage … and new regulatory and compliance issues as well.
With technology changing at lightning speed, there’s a lot to learn – and not much time to learn it. If you plan to reap the benefits, listen up.
Noted Washington FDA lawyer Bradley Merrill Thompson Esq. of Epstein Becker & Green P.C. outlines what the agency has done to date … and what it plans in months to come. Over the course of 90 fast-paced minutes, he’ll fill you in on:
Smartphones and digital apps already have given consumers powerful tools to take control of their own health. The changes affecting the FDA-regulated manufacturing community will dwarf these. You need to get up to speed, and fast.
This presentation is directed at makers of drugs, biologics, medical devices and combination products. It will be particularly useful to the following executives and professionals:
Bradley Merrill Thompson Esq., Epstein Becker & Green P.C., counsels device, drug, and combination product companies on a wide range of FDA regulatory, reimbursement and clinical-trial issues. Mr. Thompson regularly defends companies receiving warning letters on subjects including good manufacturing practice, compliance and off label promotion.
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