Online CDM & PV Course With 100% Placement Assistance

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

Advanced 0(0 Ratings) 0 Students enrolled English
Created by kunal Narhare
Last updated Mon, 13-Jan-2025
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Course overview
Description

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

Start learning CDM and PV 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. Clinical Data Management (CDM) is an important phase in clinical research, which leads to the generation of high-quality, reliable, and statistically sound data from the clinical trials. 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 Dr. Rutuja Narhare 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?

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.

What will i learn?

  • Become a Clinical Data Management and Pharmacovigilance Professional and work with world's leading Contract Research Organisations.
  • Understand more about adverse drug reactions
  • Get familiarize with various roles in CDM and PV
Requirements
  • Ideally who has completed their graduation in science, pharmacy or ailed branch also who are interested in medicine field
Curriculum for this course
30 Lessons 13:47:12 Hours
Introduction To Clinical Research
3 Lessons 02:34:31 Hours
  • Introduction To Clinical Research
    00:34:13
  • Terminologies Used in Clinical Cesearch
    01:25:14
  • Origin and History of Clinical Research
    00:35:04
Drug Development Process
5 Lessons 02:09:04 Hours
  • Phase-0 and Phase-|
    00:34:01
  • PHASE-II CLINICAL TRIALS
    00:17:15
  • PHASE-III CLINICAL TRIALS
    00:19:41
  • PHASE-IV CLINICAL TRIALS
    00:16:33
  • BA.BE Studies
    00:41:34
Good Clinical Practice (GCP)-ICH E6
6 Lessons 03:56:25 Hours
  • ICH GCP Principles
    00:23:43
  • INVESTIGATOR RESPONSIBILITIES
    00:39:34
  • Roles and Responsibilities IRB IEC
    00:35:38
  • Roles and Responsibilities Sponsor
    00:32:54
  • Protoccol Final
    00:49:47
  • Essential Documents
    00:54:49
Safety Reporting
3 Lessons 01:42:41 Hours
  • Pharmacovigilance and its Aims
    00:25:16
  • Adverse Event Reporting in Clinical Trials
    00:38:05
  • ADR Classification and Evolution
    00:39:20
Pharmacovigilance
5 Lessons 01:15:17 Hours
  • Overview of Pharmacovigilance
    00:18:13
  • History of Pharmacovigilance
    00:12:34
  • Aggregate Review in Pharmacovigilance
    00:10:07
  • Medical Review of ICSRs
    00:15:47
  • Naranjo Scale for Causality Assessment
    00:18:36
Clinical Data Management
8 Lessons 02:09:14 Hours
  • Code of Federal Regulations (CFR) 21 CFR PART 11
    00:20:31
  • CRF Design
    00:18:52
  • Introduction to Clinical Data Management (CDM)
    00:14:00
  • Data Entry Methods
    00:13:56
  • The Future of Clinical Data Management (CDM)
    00:08:07
  • CDM Study Start Up Activities
    00:14:11
  • CDM Study Conduct Activities
    00:26:01
  • CDM Study Closeout Activities
    00:13:36
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About instructor

kunal Narhare

6 Reviews | 20 Students | 10 Courses
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