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Course overview
You want to upgrade your skills and start career in ever
growing medical writing industry then this course is perfect for you!
Join Medical Writing Course to start your career in most
growing field of Pharma & life-Science Industry!
Either you're completely brand new to medical writing, or
you've played around it but want to get more comfortable with medical writing.
Either way, this course will be great for you.
Medical writing is the #1 field of Pharma & life-Science
Industry. This full course is the best way to learn how to implement it.
What makes me qualified to teach you?
My name is Mrs Deshpande and I've been in the medical
writing for over a Two decade. Plus I'm the creator of some of the most
popular online courses - with over 12000+ 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 medical writing 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 medical writing. So
if there is any way I can improve this course, just tell me and I'll make it
happen.
What is this Medical Writing course all about?
In this complete guide to medical writing, you'll not only
learn all of the topics and segments of medical writing, but also how to
implement in real Industry so that you can crack any interview and start your
career with a bang.
This medical writing course will cover everything you
need to know to start your career, including:
- Introduction to Medical Writing
- Introduction to Regulatory Affairs And
Regulatory Bodies
- Introduction to GCP
- Scientific Writing
- Medical Writing for Clinical Research
- Application, Approval And Quality Assurance
- Ethics in
Medical Writing
By the end of this course, your confidence as a Medical
Coder will soar. You'll have a thorough understanding of medical writing domain
for fun or as a career opportunity.
Go ahead and click the enroll button, and I'll see you in
lesson 1!
What will i learn?
- Knowledge of Medical Writing industry
- You will be job ready for Medical Writing domain
- Basics of Medical Writing and its Terminologies
- Stake holders of Medical Writing
- What is the career pathway in Medical Writing
- Process of drug development and understand different clinical trials phases
- Detail study of Good Clinical Practices
- Will be gaining profound knowledge of informed consent
- Will look at the purpose of essential document requirements
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
11:39:54 Hours
Introduction to Medical Writing
5 Lessons
00:53:27 Hours
-
Introduction to Medical Writing
00:14:01
-
Medical Writing in Clinical Research
00:13:53
-
Type of Medical Writing
00:08:55
-
Medical Writing Questions
00:06:39
-
Medical Writing as a Career
00:09:59
Introduction to Regulatory Affairs
9 Lessons
02:37:06 Hours
-
Introduction to Regulatory Affairs
00:09:41
-
International Regulations and Initiatives
00:17:18
-
FDA- An Introduction
00:20:18
-
CDSCO
00:16:30
-
Code of Federal Regulation (CFR)
00:15:10
-
CT_Rules_2019
00:30:06
-
ICMR Guidelines
00:48:03
-
MCQs Introduction to Regulatory Affairs And Regulatory Bodies
.
-
References and links for clinical research regulations
.
Good Clinical Practice (GCP)-ICH E6
10 Lessons
02:48:41 Hours
-
Responsibilities of Ethics Committee Members
00:31:35
-
Protocol and Investigator Brochure
00:06:56
-
Essential Documents
00:34:04
-
Good Clinical Practices- Notes
.
-
History Development of International Regulations in Clinical Research
00:18:14
-
Good Clinical Practices
00:12:04
-
Ethics committee
00:13:46
-
Investigator Responsibilities
00:13:40
-
Sponsor Responsibilities
00:38:22
-
Good Clinical Practices- Quiz
00:00:00
Protocol Designing
8 Lessons
02:11:48 Hours
-
CRF_Design_2
00:26:16
-
Trial Master File
00:08:01
-
E Trial Master File
00:06:44
-
Drafting a study protocol
00:30:56
-
Study Design
00:27:58
-
Informed Consent
00:31:53
-
Design of Trial- Notes
.
-
Protocol Designing- Quiz
00:00:00
Scientific Writing
4 Lessons
01:02:19 Hours
-
Scientific Writing
00:26:41
-
Abstract Writing
00:12:37
-
Paper Writing
00:10:39
-
Writing Research Proposal
00:12:22
Application and Approvals
5 Lessons
01:32:24 Hours
-
Purpose of QA Documentation
00:26:59
-
Responsibilities of Quality Functions
00:13:24
-
Application of Permission
00:15:29
-
Approval of Clinical Trial
00:13:13
-
Medical Devices
00:23:19
Ethics in Medical Writing
3 Lessons
00:34:09 Hours
-
Legal & Ethical Issues in Medical Communication
00:08:37
-
Research and Ethics I
00:12:09
-
Research and Ethics II
00:13:23
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