The Investigational Medicinal Product Dossier Conference

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 Applications

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

Contact Detail:

Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]
http://www.compliance4all.com/
Event Link : http://www.compliance4all.com/control/w_product/~product_id=501059LIVE?channel=mailer&camp=Webinar&AdGroup=govevents_Jan_2017_SEO
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