PRACTICAL HANDBOOK OF DRUG REGULATORY AFFAIRS-I (M PHARMACY FIRST SEMESTER)

The primary objective of this book is to serve as an indispensable resource for students who are aspiring to excel in the realm of pharmaceutical regulatory affairs. With the pharmaceutical industry becoming increasingly complex and tightly regulated, it is essential for students to have access to a practical and up-to-date handbook that can help them navigate the intricacies of this field.
Key Features of “Practical Handbook of Drug Regulatory Affairs”:
1. Comprehensive Coverage: The handbook covers a wide range of topics related to drug regulatory affairs, including the drug approval process, regulatory submissions, compliance, and quality assurance.
2. Practical Guidance: The content is presented in a practical and user-friendly manner, with clear explanations, examples, and case studies to help students apply regulatory concepts in real-world scenarios.
3. Updated Information: The book incorporates the latest regulations, guidelines, and industry best practices to ensure that students are well-prepared for the evolving landscape of drug regulatory affairs.
4. Student-Focused Approach: “Practical Handbook of Drug Regulatory Affairs” is tailored to meet the specific needs of M.Pharm Semester 1 students, providing them with the knowledge and skills necessary to excel in their coursework and future careers.