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Clinical Trial eAlert Articles
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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