Advanced Certificate in Drug Development Lifecycle Planning
-- ViewingNowThe Advanced Certificate in Drug Development Lifecycle Planning is a comprehensive course designed to provide learners with critical skills in drug development. This certification focuses on strategic planning, regulatory affairs, clinical trial management, and market access, ensuring a deep understanding of the entire drug development lifecycle.
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⢠Introduction to Drug Development Lifecycle: Overview of the drug development process, including key stages and regulatory considerations.
⢠Target Identification and Validation: Techniques for identifying and validating drug targets, including genomic and proteomic approaches.
⢠Lead Selection and Optimization: Methods for selecting and optimizing lead compounds, with a focus on medicinal chemistry and ADME properties.
⢠Preclinical Development: Strategies for preclinical testing, including in vitro and in vivo models, toxicology assessment, and pharmacokinetics.
⢠Clinical Trials Design and Conduct: Overview of clinical trial phases, study designs, and regulatory requirements for conducting clinical trials.
⢠Regulatory Affairs and Submissions: Regulatory frameworks for drug development, including IND, NDA, and MAA submissions.
⢠Intellectual Property and Commercialization: Intellectual property strategies for drug development, including patents, licensing, and collaborations.
⢠Quality Assurance and Control: Quality assurance and control strategies for drug development, including GMP, GLP, and GCP.
⢠Project Management in Drug Development: Project management principles and tools for drug development, including risk management, budgeting, and timelines.
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