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Executive Certificate in Drug Repurposing and Regulatory Affairs

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Drug Repurposing: Transform existing medications into new treatments. This Executive Certificate equips you with expert knowledge in drug repurposing strategies and regulatory pathways.

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์ด ๊ณผ์ •์— ๋Œ€ํ•ด

Learn about clinical trial design, regulatory submissions (NDA, ANDA), and intellectual property. Ideal for pharmaceutical professionals, researchers, and regulatory experts seeking career advancement. Gain a competitive edge in the rapidly evolving field of drug development and commercialization. Master data analysis and market access strategies for repurposed drugs. Accelerate your career in this exciting and impactful area. Explore the program today and register now!

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๊ณผ์ • ์„ธ๋ถ€์‚ฌํ•ญ

  • Introduction to Drug Repurposing: Opportunities and Challenges
  • Regulatory Landscape of Drug Repurposing: FDA Guidelines and International Regulations
  • Drug Discovery and Development Process: Adaptation for Repurposing
  • Preclinical Studies and Data Analysis for Repurposed Drugs
  • Clinical Trial Design and Execution in Drug Repurposing
  • Intellectual Property and Licensing in Drug Repurposing
  • Pharmacovigilance and Post-Market Surveillance for Repurposed Drugs
  • Case Studies in Successful Drug Repurposing
  • Business and Commercialization Strategies for Repurposed Drugs
  • Ethical Considerations and Patient Advocacy in Drug Repurposing

๊ฒฝ๋ ฅ ๊ฒฝ๋กœ

Career Role Description Drug Repurposing Scientist (UK) Research and develop new therapeutic uses for existing drugs, focusing on regulatory compliance.

High demand for expertise in drug discovery and development.

Regulatory Affairs Specialist (Pharmaceutical) Ensures compliance with regulations governing drug development and marketing.

A crucial role involving drug repurposing submissions and lifecycle management.

Clinical Research Associate (CRA) - Drug Repurposing Trials Oversees clinical trials for repurposed drugs, ensuring ethical and regulatory standards.

Requires strong understanding of clinical trial protocols and regulatory guidelines.

Pharmacovigilance Scientist (Drug Safety) Monitors the safety of repurposed drugs after market authorization.

A vital role in post-market surveillance and risk management.

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์ƒ˜ํ”Œ ์ธ์ฆ์„œ ๋ฐฐ๊ฒฝ
EXECUTIVE CERTIFICATE IN DRUG REPURPOSING AND REGULATORY AFFAIRS
์—๊ฒŒ ์ˆ˜์—ฌ๋จ
ํ•™์Šต์ž ์ด๋ฆ„
์—์„œ ํ”„๋กœ๊ทธ๋žจ์„ ์™„๋ฃŒํ•œ ์‚ฌ๋žŒ
London School of International Business (LSIB)
์ˆ˜์—ฌ์ผ
05 May 2025
๋ธ”๋ก์ฒด์ธ ID: s-1-a-2-m-3-p-4-l-5-e
์ด ์ž๊ฒฉ์ฆ์„ LinkedIn ํ”„๋กœํ•„, ์ด๋ ฅ์„œ ๋˜๋Š” CV์— ์ถ”๊ฐ€ํ•˜์„ธ์š”. ์†Œ์…œ ๋ฏธ๋””์–ด์™€ ์„ฑ๊ณผ ํ‰๊ฐ€์—์„œ ๊ณต์œ ํ•˜์„ธ์š”.
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