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FDA Pharmaceutical and Medical Device Audioconferences

Drug Repositioning:
Successful Strategies to Extend the Product Life Cycle Four Case Studies

An FDAnews audioconference
Monday,  Aug.  25,  2008  •  1:30 p.m.  - 3:00 p.m. 

No Longer Approvable or Not-approvable:
What the FDA’s New Response to Drug Applications Really Means

An FDAnews audioconference
Tuesday,  Aug.  26,  2008  •  11:00 a.m.  - 12:30 p.m. 

The EPA’s New Clean Air Initiative for Pharma:
Who Will Follow Pfizer?

An FDAnews audioconference
Wednesday,  Aug.  27,  2008  •  1:30 p.m.  - 3:00 p.m. 

Medical Device Supplier Audits
What a Former FDA Official Can Tell You About Third-Party Monitoring

An FDAnews audioconference
Thursday,  Sept.  4,  2008  •  1:30 p.m.  - 3:00 p.m. 

Third-Party Inspections:
Saving Devicemakers Time and Money

An FDAnews audioconference
Tuesday,  Sept.  9,  2008  •  1:30 p.m.  - 3:00 p.m. 

Indemnification Clauses Under Clinical Trial Agreements

An RxTrials Institute audioconference
Wednesday,  Sept.  10,  2008  •  11:00 a.m.  - 12:30 p.m. 

The FDA's New Manufacturing Rules for Investigational Drugs:
Sept. 15 Compliance Deadline Is Looming

An FDAnews audioconference
Wednesday,  Sept.  10,  2008  •  1:30 p.m.  - 3:00 p.m.