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Overview of Regulatory Pathways and Timelines for Small Drug Molecules & Medical devices
Dr. Yashashwini Reddy
June 15, 2024
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Regulatory Affairs
Navigating the Premarket Notification (510(k)) Process: A Guide to FDA Approval
Dr. Yashashwini Reddy
June 15, 2024
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Regulatory Affairs
Global expedited Regulatory Pathways
Dr. Yashashwini Reddy
June 14, 2024
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Regulatory Affairs
What is a Batch Manufacturing Record
Dr. Yashashwini Reddy
June 13, 2024
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Production Department
The FDA Investigational New Drug (IND) Review Process: Key Steps and Insights
Dr. Yashashwini Reddy
June 12, 2024
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Regulatory Affairs
What are the Methods in Pharmacovigilance
Dr. Yashashwini Reddy
June 10, 2024
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Pharmacovigilance
What are Clinical trials?
Dr. Yashashwini Reddy
June 10, 2024
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Clinical Research
What is Trial Master File ?
Dr. Yashashwini Reddy
June 8, 2024
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Clinical data Management
What is the importance of diluents in tablet Compression
Dr. Yashashwini Reddy
June 7, 2024
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Research & Development
CTD- Common Technical Document
Dr. Yashashwini Reddy
June 6, 2024
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Regulatory Affairs
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