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Peddehapu Pavani is noted for her contributions to the field of pharmaceutical regulations, particularly concerning non-prescription drugs. Her works, including "MARCO REGULADOR DE LOS MEDICAMENTOS DE VENTA SIN RECETA EN EE.UU. E INDIA" and "REGULATORY FRAMEWORK FOR NON-PRESCRIPTION DRUGS IN U.S & INDIA," present a thorough analysis of the regulatory environments in the United States and India. These texts provide insights into how different regions handle the sale and distribution of over-the-counter medications, emphasizing the importance of regulatory frameworks in ensuring public safety and effective healthcare delivery.

Through her research and writings, Pavani has shed light on the complexities of pharmaceutical regulations, which can vary significantly from one country to another. Her work not only informs policymakers and healthcare professionals but also serves as a resource for students and scholars interested in the intersection of law, health, and medicine. By addressing the challenges and opportunities within the regulatory landscape, she contributes to a better understanding of how to navigate these systems effectively.