A Must Webinar: eSource and the Paperless Clinical Trial

 

 

Target Health is pleased to announce that Dr. Jules T. Mitchel will be running a Webinar, sponsored by FDANEWS, on the topic of “eSource and the Paperless Clinical Trial.“ The 90 minute Webinar will take place this Tuesday at 1:30.

 

Finally, in the clinical trial arena, the the R. Buckminster Fuller mantra of “doing more with less“ has arrived. Less paper equals more productivity, reduced time to the market and a greener world. If you’re looking to decrease onsite monitoring, decrease data entry transcription errors, decrease time to database lock, etc. now is your chance to learn how. Here are just a few of the specifics of the Webinar:

 

  • Source records: What they are, and the FDA’s perspective
  • Complying with FDA’s proposal for direct data entry
  • Paper backups for electronic records – the risks and the rewards
  • Impact of direct data entry on clinical research and data management
  • Paradigm shift: Product development and direct data entry
  • Impact of companies providing monitoring, data management and EDC services
  • And much more

For more information about Target Health contact Warren Pearlson (212-681-2100 ext. 104). For additional information about software tools for paperless clinical trials, please also feel free to contact Dr. Jules T. Mitchel or Ms. Joyce Hays. The Target Health software tools are designed to partner with both CROs and Sponsors. Please visit the Target Health Website,

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