Patient Experience Comes to Drug Development

In this ISSUE

Latest in Business and People News

MyStudies Platform Brings Patient Experience to Drug Development

Too Fast or Too Slow? Debate Intensifies over FDA Regulatory Requirements

Artificial Intelligence

AI Mitigates Clinical Trial Placebo-Response

Dominique Demolle, CEO of Tools4Patient, discusses the effect artificial intelligence is having on the statistical impact of clinical trial placebo response.
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Watch Donald A. Deieso, PhD discuss challenges WCG addresses.

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Sponsored by: WCG

EMA

Getting Ready for Godot: Rehearsals for Europe's New Clinical Trials Rules

Peter O'Donnell discusses the European Commission's compendium and how triallists are not only obliged to comply with the current rules, but at the same time to prepare themselves for the future rules.
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Calendar

/ 3^rd Annual Medical Writers Summit — 9/25–9/26 /

/ 4^th Annual Lay Summaries Summit — 9/25–9/26 /

Therapeutic Specific Areas

CMC Considerations for Gene Therapy and Regenerative Medicine Studies

The unforeseen challenges with clinical trial execution in gene therapy and regenerative medicine studies, such as unchanging FDA regulations, discussed.
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eClinical

eClinical Technology Considerations for Cell and Gene Therapy Studies: Case Study Snapshots of Personalized Medicine

With the world of gene therapy still rapidly evolving, an Interactive Response Technology system might help a sponsor navigate new and complex steps throughout the supply chain.
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Patient Centricity

Patient Experience Comes to Drug Development

Irfan Khan, writes that though we celebrate MyStudies' teams work, the FDA's Patient Engagement Advisory Council deserves specific credit for bringing the patient voice into the design thinking for technologies in clinical research.
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Lisa Henderson
Editor in Chief
LHenderson@mmhgroup.com

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Todd Baker
Group Publisher
tbaker@mmhgroup.com

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