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Introduction:

Pharmacovigilance is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. It plays a crucial role in ensuring the safety and efficacy of pharmaceutical products once they are on the market. Post-marketing surveillance is an essential component of pharmacovigilance, as it involves monitoring the safety of drugs after they have been approved for use by regulatory authorities.

Chapter 1: Introduction
1.1 Introduction
1.2 Background of study
1.3 Problem Statement
1.4 Objective of study
1.5 Limitation of study
1.6 Scope of study
1.7 Significance of study
1.8 Structure of the Thesis
1.9 Definition of terms

Chapter 2: Literature Review
2.1 Overview of pharmacovigilance
2.2 History of pharmacovigilance
2.3 Importance of pharmacovigilance in public health
2.4 Regulatory frameworks for pharmacovigilance
2.5 Methods of pharmacovigilance
2.6 Challenges in pharmacovigilance
2.7 Role of healthcare professionals in pharmacovigilance
2.8 Role of patients in pharmacovigilance
2.9 Pharmacovigilance in developing countries
2.10 Future trends in pharmacovigilance

Chapter 3: Research Methodology
3.1 Research design
3.2 Data collection methods
3.3 Data analysis
3.4 Sample selection
3.5 Ethical considerations
3.6 Limitations of the study
3.7 Validity and reliability
3.8 Scope of generalizability

Chapter 4: Discussion of Findings
4.1 Overview of findings
4.2 Analysis of data
4.3 Comparison with existing literature
4.4 Implications of findings
4.5 Recommendations for future research
4.6 Policy implications
4.7 Practical implications
4.8 Contributions to the field

Chapter 5: Conclusion and Summary
5.1 Summary of key findings
5.2 Conclusion
5.3 Contributions to the field
5.4 Recommendations for future research

Thesis Overview:

Pharmacovigilance and post-marketing surveillance of drugs are crucial aspects of ensuring the safety and efficacy of pharmaceutical products. This thesis aims to provide a comprehensive overview of the field, starting with an introduction that discusses the background of the study, the problem statement, the objectives, limitations, scope, significance, and structure of the thesis. The literature review covers various topics related to pharmacovigilance, including its history, importance, regulatory frameworks, methods, challenges, roles of healthcare professionals and patients, and future trends.

The research methodology chapter details the research design, data collection methods, analysis, sample selection, ethical considerations, limitations, validity, reliability, and scope of generalizability. The discussion of findings chapter presents an analysis of the data, comparisons with existing literature, implications, recommendations for future research, policy implications, practical implications, and contributions to the field. Finally, the conclusion and summary chapter summarizes the key findings, conclusions, contributions, and recommendations for future research.

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