This book offers an in-depth examination of legal frameworks governing pharmaceutical transactions, product safety, and liability across different jurisdictions. The book analyzes the intersection between contractual obligations, tort-based liability, and public health regulations in the life sciences sector. It explores key issues such as clinical trial agreements, drug manufacturing contracts, patient safety, and compliance with international regulatory bodies like the EMA and FDA. Comparative insights from European, American, and Asian legal systems highlight variations in risk allocation,...