Drug Discovery & Development in the Pharmaceutical Industry

Categories: Manufacturing, Paid Course
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About Course

The Drug Discovery and Development course offered by Pharmastate Academy covers a comprehensive range of topics essential for understanding the intricate process of bringing new medications to market. Through a multidisciplinary approach, students delve into scientific research, technological advancements, and regulatory procedures crucial for drug development. From identifying potential drug targets to conducting preclinical and clinical trials, the course explores every stage of the drug discovery journey. Participants gain insights into disease mechanisms, techniques for studying them, and strategies for target identification. 

With a focus on practical applications, students learn about high-throughput screening techniques, hit-to-lead optimization, structure-activity relationship studies, and pharmacokinetics/pharmacodynamics optimization. Regulatory approval processes and post-market surveillance methods are also thoroughly discussed, ensuring students grasp the entire lifecycle of pharmaceutical development. Engaging and informative, this course equips learners with the knowledge and skills necessary for success in the dynamic field of drug discovery and development.

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What Will You Learn?

  • Fundamental stages and importance of drug discovery and development.
  • Techniques for target identification and validation in the drug development process.
  • Lead discovery and optimization strategies to develop potential drug candidates.
  • Essential steps of preclinical and clinical development, including safety and efficacy assessment.
  • Insights into the regulatory approval process and post-market surveillance of pharmaceuticals.

Course Content

1. Drug Discovery & Development in the Pharmaceutical Industry

  • 1.1 Objectives
    02:49
  • Quiz: Introduction

2. Target Identification

3. Target Validation

4. Lead Discovery

5. Lead Optimization

6. Preclinical Development

7. Clinical Studies

8. Regulatory Approval

9. Post-Market Surveillance

10. Final Assessment

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