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The Investigational Medicinal Product Dossier Usa 2017 webinar by Compliance4all

  November 17, 2016  
Compliance4All, Online

This 90 minute training course will provide your company the opportunity 

for comprehensive understanding of the IMPD (Investigational Medicinal 

Product Dossier) and the structure and content differences between a EU 

CTA Application and an FDA IND Application.

Why you should attend: 
All sponsors, CROs, Sites and auditors of Clinical Research who are 

involved in pharmaceutical or biological development need to possess the 

knowledge and be efficient in completing successful applications for their 

studies. Knowing what is expected of you and "getting-it-right" the first 

time, will allow faster development of innovative products. 

Areas Covered In the Session:
    US FDA and EU Agency Orientation / Structure
    Start –Up and Conducting Clinical Trial Processes
    Following Product Registration / Licensing Options
    Company Strategy- Linking Clinical Trials & Marketing Authorization 


Who will benefit: 
This Webinar will provide invaluable assistance to all personnel in the 

Pharmaceutical, Biotechnology and CRO industry conducting Clinical 

Trials including:
    Sponsor Senior management
    Project Managers
    Clinical Trial Heads
    Medical writers

Organized by: Compliance4All
Invited Speakers:
Speaker Profile:
Robert J. Russell For the past 9 years, Bob has been President of RJR 

Consulting, Inc. The company assists the pharmaceutical, medical device 

and biotech industries in understanding and complying with International 

Regulations affecting compliance, new product development, 

manufacturing and quality assurance. RJR has offices in Columbus, OH, 

Washington, DC, Brussels, Belgium with exclusive affiliates across Asia 

and Latin America.
Deadline for Abstracts: 2017-01-23
Contact Detail:

Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
Twitter Follow us – https://twitter.com/compliance4all
Facebook Like us – https://www.facebook.com/Compliance4all
LinkedIn Like us – https://www.linkedin.com/company/compliance4all
E-mail: support@compliance4All.com
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