Online Diploma in Pharmacovigilance with 100% Placement

Join the best online pharmacovigilance course with placement. Learn job oriented skills about GCP-ICH, Clinical Research, Safety Reporting, Drug Development Process, Pharmacovigilance & Etc.

Beginner 5(8 Ratings) 89 Students enrolled English
Created by Vaishali Deshpande
Last updated Mon, 01-Apr-2024
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Course overview

Online Pharmacovigilance Course Details:

Pharmacovigilance is the science of drug safety, plays a crucial role in safeguarding patient well-being and building trust in medical treatments. It ensures the safety of medications throughout their lifecycle is paramount in healthcare. Join our comprehensive online Pharmacovigilance course and emerge as a guardian of drug safety!

TechnoBridge offers the best online pharmacovigilance course with 100% placement. We have a 27+ years industry expert trainers they have designed a detailed curriculum as per the real time industry needs. We conduct time to time doubt clearing sessions in that session every student gets proper individual chance to discuss with our trainer. We also have experienced placement team; they have a strong relationship with many pharmacovigilance organizations to provide interview call to students. Our online pharmacovigilance course all the important aspects of pharmacovigilance like GCP-ICH, Clinical Research,  Safety Reporting, Drug Development Process, Pharmacovigilance & Etc.

Course Objective:

  • Equip you with the knowledge and skills to excel in the field of pharmacovigilance.
  • Master the fundamentals of drug safety monitoring and risk management.
  • Develop expertise in identifying, reporting, and analyzing adverse drug reactions (ADRs).
  • Understand the regulatory landscape and navigate pharmacovigilance guidelines.
  • Gain practical experience through case studies, assignments, and mock interviews.
  • Be prepared for a rewarding career in this diverse and ever-evolving field.

    How to Enroll in Pharmacovigilance Course?

    Ready to start your pharmacovigilance journey? Simply visit our website and click the "Register Now" button on the course page. Fill out the application form, and our friendly team will be in touch to guide you through the process.

    Eligibility for Pharmacovigilance Course:

    This course welcomes individuals with a scientific background and a passion for patient safety. We cater to graduates in Life Sciences (B.Sc./M.Sc. Biotechnology,  Microbiology, Nursing, B.Pharm/ M.Pharm etc.) and allied disciplines. No prior experience in pharmacovigilance is required, but a strong foundation in science and analytical skills is beneficial.

    Pharmacovigilance Course Fee Structure:

    We believe education should be accessible to all. Therefore, we offer flexible fee structures to suit your needs:

    • Full payment: For one time payment its 20000/-.
    • Installment options: For 2 installments its 22000/-.

    Course Methodology:

    Our interactive online learning approach ensures you get the most out of your studies:

    • Doubt Clearing Sessions: We conduct time to time doubt clearing sessions so every candidate can clear their
    • Mock interviews: Gain confidence and prepare for job interviews with personalized feedback.
    • Unlimited placement support: Benefit from our dedicated placement team that connects you with top companies in the field.

    Learning Outcomes:

    • Understand the principles and practices of pharmacovigilance in the pharmaceutical industry.
    • Identify and report ADRs effectively using recognized tools and frameworks.
    • Analyze pharmacovigilance data and contribute to risk management strategies.
    • Navigate the regulatory landscape and comply with international guidelines.
    • Develop communication and teamwork skills essential for pharmacovigilance careers.
    • Be prepared to pursue various rewarding opportunities in the pharmacovigilance field.

    Why Choose TechnoBridge for Pharmacovigilance Course?

    • Industry-experienced faculty: Learn from renowned experts with extensive practical experience in pharmacovigilance.
    • Comprehensive curriculum: Master all aspects of pharmacovigilance from theory to practical application.
    • Live online learning: Interact with instructors and peers in real-time for a dynamic learning experience.
    • Career-focused guidance: Get personalized assistance with resume writing, interview preparation, and job placement.
    • Affordable and flexible fee structure: Choose from various payment options to fit your budget.
    • Lifetime access to course materials: Continue learning and revisiting key concepts even after course completion.

    Career Opportunities:

    The booming pharmacovigilance field offers a plethora of exciting and well-paying careers. With our comprehensive training, you can pursue fulfilling roles in diverse areas, including:

    • Clinical Research Associate (CRA)
    • Pharmacovigilance Specialist
    • Medical Writer:
    • Drug Safety Officer:

    What will i learn?

    • Become a Pharmacovigilance Professional and work with world's leading Contract Research Organisations.
    • Understand more about adverse drug reactions
    • Get familiarize with various roles in Pharmacovigilance
    Requirements
    • Ideally who has completed their graduation in science, pharmacy or ailed branch also who are interested in medicine field
    Curriculum for this course
    44 Lessons 08:55:39 Hours
    Introduction to Clinical Research
    6 Lessons 01:11:24 Hours
    • Responsibilities of Ethics Committee Members
      00:31:35
    • Introduction to Clinical Research
      00:15:29
    • Terminologies in Clinical Research
      00:16:32
    • Advantages of CR in India
      00:07:48
    • Introduction to Clinical Research- Notes
      .
    • Introduction to Clinical Research Quiz
      00:00:00
    Drug Development Process
    9 Lessons 01:49:25 Hours
    • Overview of Drug Development
      00:22:54
    • Clinical Trial Phase 0
      00:04:05
    • Clinical Trial Phase I
      00:19:41
    • Clinical Trial Phase II
      00:10:57
    • Clinical Trial Phase III
      00:15:33
    • Clinical Trial Phase IV
      00:17:26
    • BA/BE Studies
      00:18:49
    • Drug Development Notes
      .
    • Data Management- Quiz
      00:00:00
    Good Clinical Practices (GCP)- ICH E6
    10 Lessons 02:48:41 Hours
    • History Development of International Regulations in Clinical Research
      00:18:14
    • Good Clinical Practices
      00:12:04
    • Ethics Commitee
      00:13:46
    • Responsibilities of Ethics Committee Members
      00:31:35
    • Investigator Responsibilities
      00:13:40
    • Sponsor Responsibilities
      00:38:22
    • Protocol and Investigator Brochure
      00:06:56
    • Essential Documents
      00:34:04
    • Good Clinical Practices- Notes
      .
    • Good Clinical Practices- Quiz
      00:00:00
    Safety Reporting
    12 Lessons 01:15:23 Hours
    • Adverse Event Reporting
      00:22:38
    • Recording of Event
      00:11:15
    • Medical Management of Adverse Events
      00:09:43
    • Handling Death
      00:04:22
    • Unblinding of Drug
      00:02:47
    • Clinical Safety and Pharmacovigilance
      00:24:38
    • E2A- Clinical Safety and Data Management
      .
    • Media 436
      .
    • Naranjo Assessment
      .
    • Order and Formulate to Determine the Quantum
      .
    • SAE Reporting
      .
    • Safety Reporting- Quiz
      00:00:00
    Pharmacovigilance
    7 Lessons 01:50:46 Hours
    • Medical Assessment -1
      00:15:29
    • Medical Assessment -2
      00:30:15
    • Overview of Pharmacovigilance
      00:14:23
    • History of Pharmacovigilance
      00:10:44
    • ADR Classifications
      00:16:54
    • Introduction to Aggregate Reporting
      00:07:27
    • AE_SAE Reporting Process
      00:15:34
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    About instructor

    Vaishali Deshpande

    90 Reviews | 780 Students | 15 Courses
    Student feedback
    5
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    Reviews

    • Naval Rathi
      The curriculum was very detailed, informative and educative. Collected a lots of knowledge about pharmacovigilance.
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    • Harshali Dond
      Excellent
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