Browse 4 Public Service courses in USA
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Public Service
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Risk Based Internal Auditing - Establishing the Methodology
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Online Webinar by
Compliance4All
Overview: The training program will focus on the establishment of a framework or methodology for RBIA and examine how to utilize risk-based questions within the process steps. Why should you Attend: The ...
Online
USD 150.00
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Overview: The training program will focus on the establishment of a framework or methodology for RBIA and examine how to utilize risk-based questions within the process steps. Why should you Attend: The ...
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How to Establish an Effective IT Governance, Risk and Compliance (GRC) Framework - Organization and Responsibilities
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Online Webinar by
Online Compliance Panel
This training program will discuss how to develop a great GRC program that ensures proper governance, risk management and compliance management of all IT systems and processes that support the business ...
Online
USD 200.00
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This training program will discuss how to develop a great GRC program that ensures proper governance, risk management and compliance management of all IT systems and processes that support the business ...
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HIPAA Security 2018 and Beyond | HIPAA Denver Seminars
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Seminar by
GlobalCompliancePanel
Overview: This lesson will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order as HIPAA is now fully enforced and the government is not using kid ...
fremont
USD 1,495.00
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Overview: This lesson will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order as HIPAA is now fully enforced and the government is not using kid ...
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Phase I Investigational Drug Products | USA Seminar 2018
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Seminar by
GlobalCompliancePanel
Overview: In January 2006, FDA issued a final rule which specified that most pharmaceutical products (including biologics) produced for use in Phase I clinical trial studies were exempted from complying ...
fremont
USD 1,495.00
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Overview: In January 2006, FDA issued a final rule which specified that most pharmaceutical products (including biologics) produced for use in Phase I clinical trial studies were exempted from complying ...
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