The Post Graduate Diploma in Clinical Research syllabus at Institute of Good Manufacturing Practices India, Noida is designed to provide overall knowledge to the students with a strong foundation. Post Graduate Diploma in Clinical Research faculty at Institute of Good Manufacturing Practices India specially focus on in-depth learning to relevant subjects. At first semester syllabus of Post Graduate Diploma in Clinical Research at Institute of Good Manufacturing Practices India, students learn the basics of programme. A strong foundation is very important for comprehensive learning. Post Graduate Diploma in Clinical Research syllabus at Institute of Good Manufacturing Practices India, Noida maintains a balance between theoretical knowledge and practical knowledge.
Post Graduate Diploma in Clinical Research first year students at Institute of Good Manufacturing Practices India are introduced with core subjects. Then they are encouraged to explore other area for a broader perspective. Institute of Good Manufacturing Practices India, Noida also provides practical training sessions, workshops, projects, and case studies to enhance student skills. Post Graduate Diploma in Clinical Research syllabus at Institute of Good Manufacturing Practices India, Noida is also frequently updated to give industry relevant training and knowledge to students. Institute of Good Manufacturing Practices India strives to provide a nurturing environment where students can learn new skills. The hands-on training sessions at Institute of Good Manufacturing Practices India enable Post Graduate Diploma in Clinical Research students to apply knowledge and skills in a controlled environment and get required experience.
According to syllabus of Post Graduate Diploma in Clinical Research progress, students learn advanced topics and complex concepts. The Post Graduate Diploma in Clinical Research curriculum at Institute of Good Manufacturing Practices India, Noida mainly focuses on analytical and critical thinking. As the Post Graduate Diploma in Clinical Research course unfolds, students develop several important skills that increases their employability. As per syllabus of Post Graduate Diploma in Clinical Research at Institute of Good Manufacturing Practices India also includes real-life projects and internship programs. It helps students critical thinking and gives them real-world experience.
Post Graduate Diploma in Clinical Research curriculum at Institute of Good Manufacturing Practices India includes group discussions, guest lectures, case studies, and skill development workshops to enhance the learning experience. The Post Graduate Diploma in Clinical Research syllabus at Institute of Good Manufacturing Practices India aims to create well-rounded professionals equipped with the necessary skills and knowledge to succeed in their chosen fields.
Additional curriculum at Institute of Good Manufacturing Practices India
Note: Given below syllabus is based on the available web sources. Please verify with the Institute of Good Manufacturing Practices India, Noida for latest Post Graduate Diploma in Clinical Research curriculum.
The Diploma in Clinical Research program offers a comprehensive education in the principles and practices of clinical research. Students embark on a journey through various crucial subjects that form the bedrock of this field. The program commences with an overview, covering historical context, ethical considerations, and regulatory frameworks. A focus on medical terminology follows, essential for clear communication in clinical research settings. Biostatistics and Research Methodology take center stage, encompassing fundamental statistical concepts, data collection methods, and study design principles. This equips students with the ability to analyze and interpret clinical data, a critical skill in the realm of clinical research. Ethics and Regulatory Affairs form another vital module, delving into ethical guidelines, regulatory compliance, and legal aspects of clinical trials. This knowledge ensures the safety and well-being of study participants and upholds the integrity of research endeavors. Clinical Trial Management addresses practical aspects like protocol development, site selection, participant recruitment, and adverse event reporting. It empowers students to proficiently manage diverse aspects of clinical studies. Furthermore, Pharmacovigilance and Drug Safety are explored, emphasizing the detection, assessment, and prevention of adverse effects linked to pharmaceutical products. This module underscores the significance of post-market surveillance in safeguarding drug safety.
S.No | Subjects |
1 | Introduction to Clinical Research Industry and Basics of Clinical Trials |
2 | Pharmacology-Concepts and Application in clinical trials |
3 | Drug Development Process |
4 | Ethics and Ethical Guidelines for Clinical Trials and Good Clinical Practice (GCP) |
5 | Regulations Guiding the Clinical Research Industry- History and Basics of National and International Regulatory Bodies |
6 | Outsourcing Clinical Trials, functioning of Clinical Research Organisation |
7 | Virtual Clinical Trial (Role of Artificial Intelligence (AI) and Machine Learning (ML)) |
8 | Biostatistics- Concepts and Application in Drug Development and Clinical Research |
9 | Clinical Trials- Phases and Trial Designs |
10 | Documentation and Data Management in Clinical Trials |
11 | Safety Reporting Techniques and Pharmacovigilance |
12 | Quality Control and Clinical Trial Management |
13 | Clinical Trials- Medical Devices |
14 | Protocol Writing and Designing |
15 | Clinical Trials -Latest updates: New Drugs and Clinical Trials Rules, 2019 |
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