Netzealous LLC DBA - Compliance4All, Online
2018-05-18
Overview: The webinar will also discuss how to make determinations of whether an adverse event is probably related, possibly related, or possibly/probably not related to a drug or device.
Why should you Attend: Are you being cited for failure to report safety information, changes to the research plan, or protocol deviations/violations or noncompliance to the sponsor or the IRB?
Areas Covered in the Session: FDA Regulations Overview of recent changes in regulatory framework GCP R2 Guidelines FDA guidance on electronic source documentation FDA BIMO Program Quality Management of Data Enhancing Excellence in conduct of Clinical Trials
Who Will Benefit: Clinical Research Investigators Research Nurses Research Managers Clinical Research Associates (CRAs) Clinical Research Coordinators Compliance Officers
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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