Investigational Product Accountability Best Practices Webinar training seminars presented by Online Compliance Panel register now on FindaSeminar.com
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Investigational Product Accountability Best Practices Webinar  
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Online Compliance Panel   

For:

Human Subjects Research, Healthcare interested in exploring the field of Clinical Research, Clinical Research Coordinators, Associates, and Managers, Administration in charge of Clinical Research, Clinical Research Sites, Contract Research Organizations, Regulatory Coordinators, Principal Investigator positions, Sub-Investigators, Pharmacists

Cost:   
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Seminar Summary:

This webinar will help clarify information to provide a foundation from which those responsible for investigational product accountability can build to avoid compliance issues and audit errors. (see full course description)
 

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Training Course Syllabus:


Investigational Product Accountability Best Practices

Objectives of the Presentation

Discuss the regulatory framework
Become familiar with investigational product best practices
Understand when a product is investigational
Know the research site´s responsibility

Why Should you Attend

This webinar will help clarify information to provide a foundation from which those responsible for investigational product accountability can build to avoid compliance issues and audit errors.

Areas Covered

21 CFR 312
21 CFR 812
Good Clinical Practice guideline requirements study conduct
Requirements under an Investigational New Drug Number
Tracking methods to assist with investigational product accountability
Areas that can create audit findings

Seminar Summary:

This webinar will help clarify information to provide a foundation from which those responsible for investigational product accountability can build to avoid compliance issues and audit errors. (see full course description)

print this agenda print agenda for the Investigational Product Accountability Best Practices Webinar training seminar

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