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Aug 16
2010

No. 12: PI Bears Heavy Responsibility in Medical-Device Study

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Jul 19
2010

No. 11: Why it's best to respond in writing to FDA's Form 483

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Jul 12
2010

No. 10: Is an IND necessary for pregabalin and paclitaxel studies

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Jul 05
2010

No. 9: What to do when the researcher is the only study subject

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Jun 28
2010

No. 8: Who is responsible for an IND annual report?

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Jun 21
2010

No. 7: When is an IND necessary?

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Jun 14
2010

No 6: Conducting a Multi-Site Trial with Individual IND Applications

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Jun 07
2010

No 5: Why It's Best to Cooperate with an Unannounced FDA Inspection

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May 31
2010

No. 4: Does Study of Botanical Product Require an IND?

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May 24
2010

No. 3: Marketed drug for cancer treatment

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May 17
2010

No 2: Medical Practice vs. Clinical Research

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May 10
2010

No 1: Faulty Transfer Triggers IND Termination

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