Professional Diploma in Pharmacovigilance - Online

Get introduced to the basic principles of Pharmacovigilance online and be harnessed with knowledge and skills required to make a successful career

Beginner 5(8 Ratings) 87 Students enrolled English
Created by Vaishali Deshpande
Last updated Thu, 01-Jun-2023
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Course overview

You want to upgrade your skills and start a career in ever-growing clinical research industry in Pharmacovigilance profiles, then this  course is perfect for you!

Start learning Pharmacovigilance to start your career in the most growing field of Pharma & life-Science Industry!

Either you're completely brand new to Clinical Research, or you've played around it but want to get more comfortable with Clinical Research. Either way, this course will be great for you.  Whereas Pharmacovigilance (PV) is also known as Drug Safety, is the pharmacological science relating to the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products. 

What makes Did I qualify to teach you?

My name is Mrs. Deshpande and I've been in the Clinical Research domain for over Two decades. Plus I'm the creator of some of the most popular online courses - with over 2000+ students like these ones:

Awesome course, easy to follow! – Radha Jaiswal

Your course is amazing, so I can say that I am learning a lot. Your English is very easy to understand ( I'm from Brazil). Thanks for sharing your amazing knowledge. – Santosh Chame

My Promise to You

I'll be here for you every step of the way. If you have any questions about the course content or anything related to this topic, you can always post a question in the course or send me a direct message.

I want to make this the best course on CDM and PV. So if there is any way I can improve this course, just tell me and I'll make it happen.

What is this CDM and PV course all about?

This online training in pharmacovigilance provides you with a groundwork in pharmacovigilance principles and operations. The program also provides training on pharmacovigilance systems, global safety standards, guidelines and regulations related  to PV. In this complete guide, you'll not only learn all of the topics and segments of CDM and PV, but also how to implement in real Industry so that you can crack any interview and start your career with a bang.

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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

84 Reviews | 685 Students | 13 Courses
Student feedback
5
8 Reviews
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Reviews

  • Naval Rathi
    The curriculum was very detailed, informative and educative. Collected a lots of knowledge about pharmacovigilance.
  • Nilesh Bhole
  • Harshada Borase
  • Harshali Dond
    Excellent
  • Prathamesh Shinde
  • Eesha Khole
  • Amruta Jadhav
  • Shubhangi Dhaygude
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