What will you learn in Drug Development Product Management Specialization Course
Understand the entire drug development lifecycle, from target discovery to commercialization.
Learn how to select drug discovery targets, perform compound screening, and design lead candidates.
Explore pre-clinical and clinical trial phases (Phase 0 to Phase 3) and New Drug Application (NDA) filing.
Gain insights into regulatory affairs, compliance, and good clinical practices (GCP).
Develop marketing, pricing, and commercialization strategies to ensure successful drug launch and patient access.
Program Overview
Course 1: Drug Discovery
⏳ 9 hours
Learn drug discovery process from target selection to IND filing.
Understand modern techniques like the lock-and-key approach, molecular biology tools, and bioinformatics.
Explore regulatory responsibilities for Investigational New Drug Applications.
Course 2: Drug Development
⏳ 9 hours
Study pre-clinical development, clinical trials, and Phase 0–3 studies.
Analyze data for efficacy and safety assessment.
Learn documentation and regulatory procedures to file a New Drug Application.
Course 3: Drug Commercialization
⏳ 9 hours
Develop marketing strategies, pricing plans, and tactical commercialization approaches.
Understand U.S. healthcare system and patient access considerations.
Apply strategic partnership and portfolio management principles to ensure commercial success.
Get certificate
Job Outlook
Prepares learners for roles such as Product Manager, Clinical Research Associate, Regulatory Affairs Specialist, and Pharmaceutical Project Manager.
Skills are highly relevant for pharmaceutical, biotech, and healthcare industries.
Understanding drug commercialization provides competitive advantage for leadership positions in life sciences.
Enhances knowledge of regulatory, clinical, and market dynamics crucial for drug development careers.
Specification: Drug Development Product Management Specialization
|
