Webinar: Patient Reported AEs using eDiary Technology

In case you missed assisTek’s Webinar on Patient Reported AE’s using eDiary Techology, you can watch it here on our website.

Please feel free to contact us with any questions at info@assisTek.com

Topics covered include:

  • Research that suggests problems with the typical AE reporting process
  • Real World Examples of Patient Reported AE’s using eDiary Technology (Phase III Global Studies)
  • System Integration (eDiary& EDC)
  • What are the Concerns?
  • What are the Benefits?

 

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Free Webinar: Patient Reported AEs using eDiary Technology: July 17th

Patient Reported Adverse Events are becoming vital to clinical trials as studies are collecting critical data from patients at home.

Join assisTek for a free webinar on  July 17, 2013 at 1:00PM EDT as we discuss Patient Reported AEs using eDiary Technology.

Description

The Webinar will discuss the following, and will conclude with an interactive Question & Answer Session:

  • Research that suggests problems with the typical AE reporting process
  • Real World Examples of Patient Reported AE’s using eDiary Technology (Phase III Global Studies)
  • System Integration (eDiary& EDC)
  • What are the Concerns?
  • What are the Benefits?

 

Date and Time

Weds, July 17, 2013 at 1:00PM EDT

Click to Register:  https://attendee.gotowebinar.com/register/8834468528499246592

Questions?

Contact Evonne Roberts, evonne.roberts@assistek.com, 480-874-9400 x. 336

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Webinar: eSource in Clinical Trials, Pros/Cons & Lessons Learned from Phase III Clinical Trials

For those of you who missed the eSource Webinar hosted by assisTek on April 4, 2013, you can still watch the entire Webinar on video below!

Description

This webinar will focus on Real-Life examples of ongoing Phase III global clinical trials using mobile Direct Clinical Data Capture (eSource) solutions. Topics discussed will include:
- Overcoming data quality and data access problems that plague studies using the traditional paper transcribed to EDC process.
- Supporting site workflow with eSource
- Cost Savings Model (Query Reduction & Elimination of SDV)
- Impact and Integration with external clinical databases (EDC, etc)

 Please contact Evonne Roberts, evonne.roberts@assisTek.com with any questions or to schedule an on-site demonstration.

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FREE WEBINAR: eSource in Clinical Trials: Pros/Cons & Lessons Learned from Phase III Global Studies

Join assisTek for a free webinar!  Details below:

Description

This webinar will focus on Real-Life examples of ongoing Phase III global clinical trials using mobile Direct Clinical Data Capture (eSource) solutions. Topics discussed will include:
- Overcoming data quality and data access problems that plague studies using the traditional paper transcribed to EDC process.
- Supporting site workflow with eSource
- Cost Savings Model (Query Reduction & Elimination of SDV)
- Impact and Integration with external clinical databases (EDC, etc)

Date and Time

Thu, Apr 4, 2013 10:00 AM – 11:00 AM MST

Register
https://attendee.gotowebinar.com/register/2003721752268355328

Questions?

Contact Evonne Roberts, evonne.roberts@assistek.com, 480-874-9400 x. 336

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