Executive Development Programme Pharma Law and Clinical Research

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The Executive Development Programme in Pharma Law and Clinical Research is a certificate course designed to provide learners with a comprehensive understanding of the legal and regulatory frameworks governing the pharmaceutical industry. This programme is crucial in a time when the pharma sector is heavily regulated, and compliance is essential for business success.

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The course addresses industry demand for professionals who can navigate the complex legal landscape of clinical research, drug development, and marketing. It equips learners with essential skills in pharmaceutical law, clinical trial management, and regulatory affairs. Upon completion, learners will be able to strategically manage legal and compliance issues, ensuring their organizations' pharmaceutical products and services meet regulatory standards. This advanced knowledge and proficiency will significantly enhance learners' career progression in the pharma sector, making them valuable assets in this rapidly evolving industry.

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โ€ข Introduction to Pharma Law
โ€ข Regulatory Affairs in Pharmaceutical Industry
โ€ข Clinical Research: Legal and Ethical Considerations
โ€ข Intellectual Property Rights and Patent Law in Pharmaceutical Industry
โ€ข Drug Approval Process and Regulations
โ€ข Advertising and Marketing Laws in Pharmaceutical Industry
โ€ข Data Privacy and Security in Clinical Research
โ€ข Import and Export Regulations in Pharmaceutical Industry
โ€ข Legal Aspects of Pharmacovigilance and Post-Marketing Surveillance

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็คบไพ‹่ฏไนฆ่ƒŒๆ™ฏ
EXECUTIVE DEVELOPMENT PROGRAMME PHARMA LAW AND CLINICAL RESEARCH
ๆŽˆไบˆ็ป™
ๅญฆไน ่€…ๅง“ๅ
ๅทฒๅฎŒๆˆ่ฏพ็จ‹็š„ไบบ
London School of International Business (LSIB)
ๆŽˆไบˆๆ—ฅๆœŸ
05 May 2025
ๅŒบๅ—้“พID๏ผš s-1-a-2-m-3-p-4-l-5-e
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