2011 - The Drug Development Process - From R&D to Commercialization - Webinar By GlobalCompliancePanel

Why you should attend: How familiar are you with the complex and cross-functional activities that make up the drug development path? If you are involved in any step of drug development from discovery research through process development, pre-clinical and toxicological testing, GMP manufacturing, clinical trials and regulatory affairs, an understanding of how your role fits in with the other activities is key to achieving effective and efficient development and commercialization.

Areas Covered In the Seminar:
The transition from discovery to development
The purpose of Pre-clinical studies
The four major clinical phases (1-4) in the drug development process and the rationale for each with key deliverables
Milestones on The "Dual Path" to Drug Commercialization
Where do IND and NDA fit into the process
Overview of the key government regulations that impact the development process (Code of Federal Regulations and ICH)
Designing the drug with the patient and regulations in mind
The criticality of effective project management for cross-functional teams during the development process with special focus on managing activities performed by contract manufactures, labs and suppliers
Who will benefit:
Research & development scientists
Clinical monitors and research associates
Medical and clinical investigators and study coordinators
Statisticians & data management professionals
CMC/pharmaceutical research professionals
Regulatory Affairs Professionals
Project Managers
Senior sales managers
Analytical Development
Program Management

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com

Phone: 800-447-9407
Fax: 302-288-6884