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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
14 Lessons
08:40:00 Hours
Introduction To Clinical Research
3 Lessons
02:34:31 Hours
-
Origin and History of Clinical Research
00:35:04
-
Terminologies Used in Clinical Cesearch
01:25:14
-
Introduction To Clinical Research
00:34:13
Drug Development Process
5 Lessons
02:09:04 Hours
-
PHASE-II CLINICAL TRIALS
00:17:15
-
Phase-0 and Phase-|
00:34:01
-
BA.BE Studies
00:41:34
-
PHASE-IV CLINICAL TRIALS
00:16:33
-
PHASE-III CLINICAL TRIALS
00:19:41
Good Clinical Practice (GCP)-ICH E6
6 Lessons
03:56:25 Hours
-
Essential Documents
00:54:49
-
Protoccol Final
00:49:47
-
Roles and Responsibilities Sponsor
00:32:54
-
Roles and Responsibilities IRB IEC
00:35:38
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INVESTIGATOR RESPONSIBILITIES
00:39:34
-
ICH GCP Principles
00:23:43
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