Why MedEvoke for Clinical Trials

Why MedEvoke for Clinical Trials

At MedEvoke, we’ve dedicated the past 2 decades to applying our unique knowledge-based scientific research analysis to our strategies providing you with a solid framework to proceed confidently. With 9 out of 10 trials failing to meet endpoints, MedEvoke’s ability to identify potential flaws and unmet needs earlier help to mitigate costly delays. We’re guided by an intrinsic motivation and purpose to help our client’s bring to market brands that help patients heal.

In Fact, we put patients in the center of all we do resulting in stronger strategic alliances that impact each phase of the trial from initiation, acceleration and optimization.

  • Social listening/engagement
  • Patient phenotype/journey
  • Site ID/training
  • Influencer ID [KOL/DOL]
  • Protocol feasibility
  • Website
  • Apps
  • Trial guide

  • Q&A bot
  • Social engagement
  • Patient portal
  • Trial call-to-action [HCP office]
  • Patient engagement
  • Trial diary/log
  • Patient/caregiver education
  • Adherence compliance strategy
  • Site Engagement
  • Data dissemination
  • Trial readout
  • Trial appreciation program
  • Site follow through
 
 
 
 
 

The MedEvoke Process for Clinical Trials

Clinical Trials are a costly endeavor.  $2.6 Billion to be exact.  There are pitfalls and obstacles with every trial and the ability to successfully navigate through the process is paramount to achieve a successful outcome.

How does MedEvoke Clinical Trials help you align your protocol framework to your desired outcomes?

It’s in our DNA.  With our diverse industry knowledgeable team, we’ve been successfully providing robust digitally-orientated medical strategy to medical affairs teams across a multitude of therapeutic categories for decades.  Unsurprisingly, these findings and insights when applied to the trial architecture can effectively impact key drivers and trial benchmarks for all stakeholders.  All while maintaining a consistent single global narrative for your brand, your pipeline, and your company.

  • Social listening/engagement
  • Patient phenotype/journey
  • Site ID/training
  • Influencer ID [KOL/DOL]
  • Protocol feasibility
  • Website
  • Apps
  • Trial guide
  • Q&A bot
  • Social engagement
  • Patient portal
  • Trial call-to-action [HCP office]
  • Patient engagement
  • Trial diary/log
  • Patient/caregiver education
  • Adherence compliance strategy
  • Site Engagement
  • Data dissemination
  • Trial readout
  • Trial appreciation program
  • Site follow through
 
 
 
 
 

Clinical Trials

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MedEvoke holds certifications from Women’s Business Enterprise National Council (WBENC), National Minority Supplier Development Council Inc (NMSDC), Small Business Administration (SBA), and Diversity Alliance for Science (DA4S).

Contact us

Phone: 908.638.5885

65 Main St.

High Bridge, NJ 08829