Entry Level Pharmacovigilance Course
Entry Level Pharmacovigilance Course, available at $19.99, has an average rating of 4.13, with 25 lectures, based on 4 reviews, and has 10 subscribers.
You will learn about Explain the basic principles and concepts of pharmacovigilance, including the importance of adverse drug reaction (ADR) reporting and how to identify and assess Comply with global regulatory requirements for pharmacovigilance, including reporting timelines, submission requirements, and reporting channels Use common pharmacovigilance tools and databases, such as VigiBase and EudraVigilance, for data collection, entry, analysis, and reporting. Manage pharmacovigilance data effectively, including data collection, entry, analysis, and reporting. Identify and manage risks associated with the use of medicinal products, including signal detection, risk assessment, and risk minimization strategies. Identify ethical considerations and challenges associated with pharmacovigilance, including confidentiality, informed consent, and data privacy Communicate pharmacovigilance information effectively to different stakeholders, and collaborate with colleagues in pharmacovigilance and other related fields t This course is ideal for individuals who are Recent graduates or individuals with a background in pharmacy, medicine, nursing, biology, or a related discipline who are interested in pharmacovigilance. Professionals working in the pharmaceutical industry who want to expand their knowledge of pharmacovigilance. Healthcare professionals, such as physicians and nurses, who are involved in prescribing or administering medicinal products. It is particularly useful for Recent graduates or individuals with a background in pharmacy, medicine, nursing, biology, or a related discipline who are interested in pharmacovigilance. Professionals working in the pharmaceutical industry who want to expand their knowledge of pharmacovigilance. Healthcare professionals, such as physicians and nurses, who are involved in prescribing or administering medicinal products.
Enroll now: Entry Level Pharmacovigilance Course
Summary
Title: Entry Level Pharmacovigilance Course
Price: $19.99
Average Rating: 4.13
Number of Lectures: 25
Number of Published Lectures: 25
Number of Curriculum Items: 25
Number of Published Curriculum Objects: 25
Original Price: ₹2,999
Quality Status: approved
Status: Live
What You Will Learn
- Explain the basic principles and concepts of pharmacovigilance, including the importance of adverse drug reaction (ADR) reporting and how to identify and assess
- Comply with global regulatory requirements for pharmacovigilance, including reporting timelines, submission requirements, and reporting channels
- Use common pharmacovigilance tools and databases, such as VigiBase and EudraVigilance, for data collection, entry, analysis, and reporting.
- Manage pharmacovigilance data effectively, including data collection, entry, analysis, and reporting.
- Identify and manage risks associated with the use of medicinal products, including signal detection, risk assessment, and risk minimization strategies.
- Identify ethical considerations and challenges associated with pharmacovigilance, including confidentiality, informed consent, and data privacy
- Communicate pharmacovigilance information effectively to different stakeholders, and collaborate with colleagues in pharmacovigilance and other related fields t
Who Should Attend
- Recent graduates or individuals with a background in pharmacy, medicine, nursing, biology, or a related discipline who are interested in pharmacovigilance. Professionals working in the pharmaceutical industry who want to expand their knowledge of pharmacovigilance. Healthcare professionals, such as physicians and nurses, who are involved in prescribing or administering medicinal products.
Target Audiences
- Recent graduates or individuals with a background in pharmacy, medicine, nursing, biology, or a related discipline who are interested in pharmacovigilance. Professionals working in the pharmaceutical industry who want to expand their knowledge of pharmacovigilance. Healthcare professionals, such as physicians and nurses, who are involved in prescribing or administering medicinal products.
This entry-level pharmacovigilance course provides an introduction to the principles and concepts of pharmacovigilance, the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems.
The course covers global regulatory requirements for pharmacovigilance, including reporting timelines, submission requirements, and reporting channels. It also explores different types of pharmacovigilance data sources, such as spontaneous reports, clinical trials, and observational studies, and how to manage this data effectively using common pharmacovigilance tools and databases.
Students will learn about the roles and responsibilities of different stakeholders in pharmacovigilance, including regulatory agencies, pharmaceutical companies, healthcare professionals, and patients. They will also explore risk management in pharmacovigilance, including signal detection, risk assessment, and risk minimization strategies.
Throughout the course, students will become familiar with pharmacovigilance terminology, abbreviations, and acronyms, and will also discuss ethical considerations and challenges associated with pharmacovigilance, such as confidentiality, informed consent, and data privacy.
Finally, the course will emphasize the importance of communication and teamwork in pharmacovigilance, and provide opportunities for students to develop these skills through group activities and case studies. Upon completion, students should be able to understand the fundamental concepts and practices of pharmacovigilance and contribute to ensuring patient safety.
Course Curriculum
Chapter 1: Overview of Pharmacovigilance
Lecture 1: Why Students should do Pharmacovigilance course
Lecture 2: Importance of Pharmacovigilance
Lecture 3: Scope of Pharmacovigilance
Lecture 4: Job Opportunities
Lecture 5: Which companies hire pharmacovigilance professionals
Lecture 6: Future Scope of Pharmacovigilance
Chapter 2: Introduction
Lecture 1: Introduction to Pharmacovigilance
Lecture 2: History Of Pharmacovigilance
Lecture 3: The Thalidomide story
Lecture 4: Role Of Pharmacovigilance in ensuring the safety of medicines
Chapter 3: Regulatory Requirements
Lecture 1: Mechanism of Action Of Medications
Lecture 2: Terminologies used in Pharmacovigilanace
Lecture 3: The Process of Reporting & Evaluating ADR
Lecture 4: Regulatory Requirements Related to Pharmacovigilance
Chapter 4: Assesment of Risk benefit & risk management plan based on PV
Lecture 1: Risk benefit & Risk management based on Pharmacovigilance data
Lecture 2: The use of Pharmacovigilance Tools & Techniques
Chapter 5: Ethical Considerations & methodologies in Pharmacovigilance
Lecture 1: Ethical Considerations related to Pharmacovigilance
Lecture 2: Methodologies Used in Pharmacovigilance
Lecture 3: Seriousness expectedness & casualty assesment
Lecture 4: Aggregate safety Reports
Chapter 6: Pharmaceutical Regulations & Signal Detection
Lecture 1: Pharmaceutical Regulations in Various countries
Lecture 2: Signal Detection & Data Mining
Chapter 7: Pharmacovigilance Databes, Softwares used
Lecture 1: Pharmacovigilance Databases
Lecture 2: Softwares used in Pharmacovigilance
Chapter 8: Process of Repoting Adverse Drug Reaction
Lecture 1: Process of Reporting an ADR
Instructors
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Dr Pravin Badhe
Founder and CEO
Rating Distribution
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- 2 stars: 1 votes
- 3 stars: 0 votes
- 4 stars: 1 votes
- 5 stars: 2 votes
Frequently Asked Questions
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