Directly.me Fundamentals of Clinical Trials – A basic learning course- Are you a health care professional or related to the field of medicine?
- Do you want to learn about the basics regarding the procedures and regulations involved in performing clinical trials of medications and treatments?
- Are you seeking an online course about this?
If this is the case then you have most certainly reached the right place. This package contains a course that has been designed to give you the basic idea about the procedures and regulations involved in performing clinical trials. This course will turn out to be very helpful to you in so many ways.

What is this course, who should take this course and what are the benefits of taking it?

Designed for students studying medicine, medical assistance or related health care fields, this course will introduce you to the procedures and regulations involved in performing clinical trials of medications and treatments. Clinical trials are an essential part of the process of developing new drugs that are then used to fight a variety of diseases, but they are also highly regulated and involve many technical and ethical aspects. In this course you will cover such topics as:
- FDA regulation of clinical trials
- Protocol development
- HIPPA
- Best practices as well as how the media affects public perception of clinical trials.
This online course is also available for credit from UCI.

Table of Contents:

- Introduction
- Protocol development and implementation
- Study site selection
- Financial controls
- Timelines
- Management of the site's operations
- Proper informed consent
- Good clinical practices compliance;
- HIPAA
- FDA regulations and guidelines
- Post-market support studies

Author Bio

Nancy Ann Schwartz will be the instructor for this course. The instructor’s teaching experience and command on this subject is expected to benefit the users.
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Fundamentals of Clinical Trials – A basic learning course
Price: Free
Availability:1 Week
Package Description

- Are you a health care professional or related to the field of medicine?
- Do you want to learn about the basics regarding the procedures and regulations involved in performing clinical trials of medications and treatments?
- Are you seeking an online course about this?
If this is the case then you have most certainly reached the right place. This package contains a course that has been designed to give you the basic idea about the procedures and regulations involved in performing clinical trials. This course will turn out to be very helpful to you in so many ways.

What is this course, who should take this course and what are the benefits of taking it?

Designed for students studying medicine, medical assistance or related health care fields, this course will introduce you to the procedures and regulations involved in performing clinical trials of medications and treatments. Clinical trials are an essential part of the process of developing new drugs that are then used to fight a variety of diseases, but they are also highly regulated and involve many technical and ethical aspects. In this course you will cover such topics as:
- FDA regulation of clinical trials
- Protocol development
- HIPPA
- Best practices as well as how the media affects public perception of clinical trials.
This online course is also available for credit from UCI.

Table of Contents:

- Introduction
- Protocol development and implementation
- Study site selection
- Financial controls
- Timelines
- Management of the site's operations
- Proper informed consent
- Good clinical practices compliance;
- HIPAA
- FDA regulations and guidelines
- Post-market support studies

Author Bio

Nancy Ann Schwartz will be the instructor for this course. The instructor’s teaching experience and command on this subject is expected to benefit the users.

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