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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Patient Reported AE’s using eDiary Technology

scdm logo

 

Recently assisTek authored an article published by the Society of Clinical Data Management’s “Data Basics”.

The article discusses the benefits of assessing AE’s in real time when the symptoms are experienced by the subject (versus during site visits only) and how the data can be integrated into existing clinical databases (including EDC).

Enjoy!

http://www.scdm.org/be-bruga/scdm/files/newsletters/databasic/2013Spring.pdf

 

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Email Alerts in Clinical Trials Improve Study Team Efficiency

Look what assisTek can do to help your study team manage compliance, undesirable events, site visits, etc more effectively and proactively! 

 Patient Non-Compliant?

  • Email alert directly to Study Team for follow-up.
  • Email reminder sent directly to patient to complete diary entry.

 

Nurse Records AE?

  • Email alert directly to Investigator for Review and Assessment.

 

Patient records undesirable symptom, event, medication, etc?

  • Email alert directly to Study Team for review and follow-up.

 

Site Visit coming up?

  • Email reminder sent directly to patient.

 

When used correctly, email alerts can help study teams manage critical issues more efficiently, and help gain compliance from patients before it’s a problem.

assisTek’s email alert system is linked directly to specific events based on protocol requirements and study team needs.

Questions about how this can work in your study? Find out more:  info@assistek.com  (and yes we do reply!)

 

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Electronic Adverse Event Reporting and Follow-up

Patient safety has never been more important than it is today in Clinical Trials.

assisTek has built an infrastructure to support the collection of patient and clinician reported adverse events, all electronically.  Emphasis has been placed on what matters most – accurate and timely reporting of symptoms, proper notification to the study team and immediate access to data.

Two relevant examples of how symptoms are captured, team members are notified, and data is updated are below:

Patient eDiary Example:  Patient reports potential Adverse Events from home, Study Team is instantly notified and has access to data for follow-up & updates.

Direct Clinical Data Capture Example:  Clinician collects Adverse Events from patient, Investigator is instantly notified and has access to data for follow-up & updates.

Contact assisTek to understand how your study can benefit.

Emailinfo@assisTek.com (and yes, we will reply!)

Also – don’t forget to Subscribe (on right toolbar) to get new postings directly to your InBox!

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