Ubiquitous Video in Pharma and e-Healthcare: Are You Ready for the US FDA?

Date : January 8th-2013
Venue : Pines Manor, NJ

Video in life sciences , it seems, is EVERYWHERE THESE DAYS !

Whether used for remote location collaboration to speed up drug clinical trials or global oversight of quality & GMP for pharmaceutical manufacturing video is becoming a strategic asset transforming key business processes. The trend where consumers are adopting tablets, smartphones or other mobile apps to assist with their own healthcare had extended the health care delivery into new territory. Integrating standards-based and easy to use video with compelling apps had become the new normal.

In this event attendees will explore:
  • Use of new technologies to accelerate clinical trials.
  • Simplifying access to experts using mobile video to support GMP inspections and protocol adherence.
  • The potential impact of the integration of mobile work flow apps into these rich media communication environments simplifies the number of devices used while supporting the BYOD trends.
Most are not aware that some applications of video however could cross that thin line between a compelling industry or consumer app open to all without industry regulation and into video based solutions that should be under US FDA oversight if used for decision-making in drug patient studies or to evaluate gaps in manufacturing processes during audits or prevent or cure disease with medical devices. Where does one end and the other begin?

On January 8th, join Polycom and FDASmart for a one-day event that will show-case compelling use of video in life sciences and when that regulatory line in the sand is crossed.

Come learn from experts that include compelling mobile video industry solutions, pharmaceutical best-of-breed application pioneers and the US FDA to learn more about the US FDA issued Mobile Apps Guidance.
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