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Issues with Consent Documents 2015
29 Oct 2015
Online Event
Home
Issues with Consent Documents 2015
Key Topics
Plain Writing
Information on Health Literacy
Increasing readability
Consent as a process
Exculpatory language
6 - 8th grade examples
What IRB reviewers like and dislike
Tips for using consent templates
Who should Attend
Clinical Research Scientists (PKs, Biostatisticians,)
Principal Investigators / Sub-investigators
Clinical Research Associates (CRAs) and Coordinators (CRCs)
Safety Nurses
QA / QC Auditors and Staff
Recruiting Staff
Human Research Protection Professionals
Clinical Research Data Managers
Read more
Past Events
Issues with Consent Documents 2015 - 29 Oct 2015, Online Event
(54383)
Issues with Consent Documents 2014 - 06 Nov 2014, Online Event
(47703)
Issues with Consent Documents 2026
Important
Please, check "Issues with Consent Documents" official website for possible changes, before making any traveling arrangements
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