Drug Development and Clinical Research
Completed by Deepali Maurya
October 16, 2026
17 hours (approximately)
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What you will learn
Explain the drug development process, clinical trial phases, and regulatory requirements in research.
Apply ICH-GCP, ethical guidelines, and clinical documentation standards in trial settings.
Analyze clinical research operations, pharmacovigilance, and compliance practices in the industry.
Skills you will gain
- Category: Drug Development
- Category: Clinical Documentation
- Category: Research
- Category: Clinical Trials
- Category: Clinical Research
- Category: Informed Consent
- Category: Good Clinical Practices (GCP)
- Category: Pharmaceuticals
- Category: Technical Writing
- Category: Communication
- Category: Clinical Research Ethics
- Category: Marketing
