Introduction

FDA has issued regulations governing IND products to protect human subjects enrolled in clinical trials. For example, in 21 CFR part 312, sponsors must submit chemistry, manufacturing and control (CMC) information on a drug or biological product as part of an IND application (§ 312.23(a)(7)).

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Venue

Online Training

Online Training, 161 Mission Falls Lane, Suite 216, Fremont, 94539, United States

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Organised by

GlobalCompliancePanel

Contact information

Mr John Robinson
161 Mission Falls Lane, Suite 216, Fremont, 94539, United States of America
8004479407
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