Sponsored by Adobe

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The Life Sciences industry can’t afford not to invest in new ways to support virtual, distributed, cross functional global teams and alliances for all aspects of R&D. Reducing costs by compromising safety or efficacy is not an acceptable prescription for a new drug launch.  However, there is a great opportunity to reduce the sting of clinical development costs associated with manual, paper-based, repetitive processes. Some examples include investigator recruitment, financial disclosure requirements, patient enrollment, and clinical supply management.  These processes are the same for every clinical trial regardless of therapeutic area or the size of the clinical trial.

You will learn how Adobe:

• provides the right enterprise solutions to accelerate your clinical development timeline and increase your profitability.
• provides an integrated approach to your Study Start-up, highlighting investigator enrollment.
• can automate your painful manual paper-based processes by:
  - reducing cycle time and increasing data quality
  - bridging the paper to digital divide
  - increasing adoption rates for greater cost efficiencies
  - meeting regulatory requirements

Featured Speakers from Adobe Life Science Solutions:

Melonie Warfel – Director, Life Sciences
Marc Eaman – Technical manager

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Coming in soon - Adobe's Rx for streamlining your Submission Process