Netzealous LLC DBA - Compliance4All, Online
2018-02-06
Overview: Learn why the single most important function of the Principal
Investigator and the study conduct team is the awareness, assessment,
and management of Adverse Events occurring during the conduct of
clinical research with drugs or devices utilizing human subjects.
Why should you Attend: With the increasing complexity of the Investigational Medicinal Products
(IMP's), it behooves all who have any role in observing Study
Participants to know the importance of accurately collecting all AE and
SAE data.
Areas Covered in the Session: How to know what an Adverse Event is and when to report it or them Knowing the AE types and likelihood of finding "rare" events Understanding laboratory AEs and the "Reference Range" concept Common Mistakes in AE / SAE Reporting
Who Will Benefit: Principal Investigators and Sub Investigators Clinical Research Scientists Safety Nurses Clinical Research Associates (CRAs) and Coordinators (CRCs) QA / QC Auditors and Staff
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com
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