Pharmacovigilance plays a crucial role in ensuring drug safety and effectiveness throughout their lifecycle. This program is designed to provide an in-depth understanding of adverse drug reactions (ADR), the principles of pharmacovigilance, and regulatory compliance. The curriculum covers historical advancements, methodologies, case processing, drug discovery, development processes, and the latest technological interventions in drug safety monitoring. With a strong emphasis on real-world applications, students will gain expertise in monitoring, assessing, and preventing adverse effects associated with pharmaceutical products.
Course Duration
40-50 Hours
Next Enrollment
March 2025
Mode of Study
Hybrid Learning
Certification
Globally Accredited Certification
Program Highlights
- General Pharmacology – Understand drug sources, administration routes, and the essential drugs concept.
- Drugs Acting on Systems – Learn about drugs affecting the nervous, cardiovascular, respiratory, endocrine, and gastrointestinal systems.
- Pharmacovigilance Principles – Gain expertise in ADR classification, spontaneous reporting, case processing, and aggregate reporting.
- Pharmacoepidemiology & Pharmacoeconomics – Study cost-effectiveness, decision analysis, health-related quality of life, and health technology assessment.
- Pharmacokinetics & Pharmacodynamics – Explore drug absorption, distribution, metabolism, excretion, receptor interactions, and dose-response relationships.
- Drug Discovery & Development – Cover target identification, preclinical and clinical development, bioequivalence trials, and regulatory requirements.
- Regulatory Frameworks – Understand international regulations, including WHO guidelines, ICH, US FDA, and EMA policies.
- Technological Advancements – Explore AI and machine learning applications in drug discovery and pharmacovigilance.
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Learning Outcomes
- Develop a thorough understanding of pharmacovigilance principles, ADR classification, and drug safety regulations.
- Master pharmacokinetics and pharmacodynamics for better drug monitoring and risk evaluation.
- Acquire expertise in drug discovery, clinical development, case processing, aggregate reporting, and regulatory compliance.
- Analyze real-world data through systematic reviews, meta-analysis, and biostatistical methodologies.
- Implement AI and machine learning tools to enhance drug safety monitoring and development.
- Gain practical knowledge through hands-on internships in regulatory safety analysis and reporting.
Why Choose Yes M Pharma?
Placement Assistance
Strong network of recruiters from the healthcare, pharmaceutical, and biotechnology industries and offer placement assistance to student
Industry Expert Trainers
Equip yourself with skills and knowledge under the mentorship of experienced faculties with over 17 years of experience in the field of healthcare research and training.
Internship Opportunities
Gain hands-on experience in safety reporting tools like Oracle Argus, systematic literature review, meta-analysis, and biostatistical analysis.
A Student’s Journey
Equip yourself with the skills and knowledge required to succeed in the healthcare, pharma, or healthcare-IT industry. Enhance your communication, personality, and technical expertise through hands-on training and real-world case studies.
Earn credentials through online or in-person programs that validate your expertise in the healthcare-IT and pharma sector. Our courses are designed to enhance your professional qualifications and provide industry-recognized certification.
Gain access to volunteer, internship, and placement opportunities in top healthcare settings like hospitals, CROs, and pharma companies. Apply real-world applications of your knowledge and kickstart your career with the right industry connections.
Receive continuous career guidance, resume-building assistance, and networking opportunities with industry professionals. Stay updated with the latest trends in healthcare, IT, and pharma to advance and grow in your career beyond placement.
Career Opportunities
Drug Safety Pharmacovigilance Career Opportunities
Career Opportunities
Drug Safety Pharmacovigilance Career Opportunities
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Drug Safety Associate
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Clinical Safety Scientist
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Pharmacovigilance Associate
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Signal Detection Analyst
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Aggregate Reporting Specialist
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Regulatory Affairs Specialist
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Pharmacovigilance Compliance
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Risk Management Specialist
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Manager
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Pharmacovigilance Trainer
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Pharmacovigilance Project Manager
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Medical Writer
Got Questions?
We Have Answers!
Explore our FAQs to find quick solutions and helpful insights.
Pharmacovigilance is the science of monitoring, detecting, and preventing adverse effects of pharmaceutical products. It ensures patient safety and regulatory compliance.
No, but a background in life sciences, pharmacy, or healthcare is beneficial. The course is designed to be accessible to beginners and professionals alike.
Yes! You will work with industry-standard tools like Argus Safety for case processing and aggregate reporting.
Graduates can work as Drug Safety Associates, Pharmacovigilance Analysts, and Regulatory Affairs Specialists in pharmaceutical companies, CROs, and regulatory agencies.
Yes, the certification is globally accredited and recognized by regulatory bodies like the USFDA, EMA, and WHO.
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