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Program

Pharmacovigilance: Concepts and Applications

Pharmacovigilance Drug Safety Adverse Drug Reactions (ADRs) Risk Management Regulatory Compliance Post-Marketing Surveillance Signal Detection Data Analysis Clinical Trials Healthcare Regulation Safety Monitoring Drug Efficacy Patient Safety Medicinal Product

Skills you will gain:

About Program:

The Pharmacovigilance: Concepts and Applications program is specifically designed for professionals in the pharmaceutical and healthcare industries who are focused on the safety and efficacy of medicinal products. This comprehensive educational initiative aims to deepen understanding and enhance skills in the field of drug safety monitoring, a critical area for public health. The program covers a broad range of topics, from the basics of pharmacovigilance, including its history and fundamental principles, to advanced modules on adverse drug reaction (ADR) identification, risk management, and regulatory compliance. Through a blend of lectures, case studies, and practical workshops, participants are equipped with the necessary tools to anticipate, identify, and mitigate risks associated with pharmaceutical products.

This program also emphasizes the practical application of pharmacovigilance in a real-world setting, bridging the gap between theoretical knowledge and practical implementation. Participants learn about the latest technologies and methodologies used in the industry, such as data mining and signal detection, which are essential for modern pharmacovigilance practices. The curriculum is designed to meet the needs of a diverse range of professionals, including pharmacists, clinical researchers, and regulatory affairs personnel, preparing them to effectively manage drug safety issues and adapt to the dynamic regulatory landscape. By the end of the program, graduates are well-prepared to lead pharmacovigilance activities, ensuring patient safety and maintaining public trust in healthcare products.

Aim:

The aim of the “Pharmacovigilance: Concepts and Applications” program is to equip healthcare professionals with the knowledge and skills necessary to monitor, assess, and enhance the safety of pharmaceutical products. The program focuses on teaching participants how to detect, analyze, and prevent adverse effects of medications, ensuring drug therapies are as safe and effective as possible. By understanding the mechanisms and methodologies of pharmacovigilance, participants will learn to mitigate risks associated with drug use, enhance patient care, and comply with global regulatory standards. The program also aims to foster a culture of continuous improvement in drug safety by integrating robust pharmacovigilance practices into the broader pharmaceutical and healthcare industries.

Program Objectives:

  • Enhance Expertise in Drug Safety Monitoring
  • Develop Skills in Risk Assessment and Management
  • Navigate Regulatory Frameworks
  • romote Ethical Practices
  • Application of Practical Tools and Techniques
  • Foster Analytical and Critical Thinking Skills

What you will learn?

1.Basic of Pharmacovigilance and Clinical Trials
2.Adverse Drug Reactions and Safety Procedure
3.Pharmacovigilance Program of India
4.Measuring impact of Pharmacovigilance Activities
5.Project Report Submission/ Article Writing

Fee Plan

INR 1999 /- OR USD 50

Intended For :

Pharmacists and Pharmacy Technicians,Clinical Researchers,Regulatory Affairs Professionals,Medical Officers and Healthcare Providers,Quality Assurance Personnel

Career Supporting Skills

Synthetic Biology Regulatory Knowledge

Program Outcomes

  1. Expert Knowledge in Pharmacovigilance
  2. Proficiency in Regulatory Compliance
  3. Advanced Risk Management Capabilities
  4. Data Analysis and Interpretation Skills
  5. Enhanced Communication Skills
  6. Ethical Decision-Making
  7. Problem-Solving Skills
  8. Operational Efficiency
  9. Career Advancement
  10. Contribution to Public Health