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Introduction to Good Clinical Practice

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Introduction to Good Clinical Practice

Dieser Kurs ist Teil von Spezialisierung „Clinical Trials: Good Clinical Practice “

Dozent: Novartis Learning

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3 Module

Verschaffen Sie sich einen Einblick in ein Thema und lernen Sie die Grundlagen.

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3 Module

Verschaffen Sie sich einen Einblick in ein Thema und lernen Sie die Grundlagen.

502 Bewertungen

Stufe Anfänger

Empfohlene Erfahrung

Flexibler Zeitplan

3 Stunden zu vervollständigen

In Ihrem eigenen Lerntempo lernen

97%

Den meisten Lernenden hat dieser Kurs gefallen

Was Sie lernen werden

Explore the clinical trial process, the basics of good clinical practice, and the history of regulatory frameworks for medical treatment and testing.

Kompetenzen, die Sie erwerben

Kategorie: Clinical Research Ethics
Kategorie: Health Equity
Kategorie: Drug Development
Kategorie: Good Clinical Practices (GCP)
Kategorie: Clinical Research
Kategorie: Clinical Trials
Kategorie: Informed Consent
Kategorie: Clinical Data Management

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10 Aufgaben

Unterrichtet in Englisch

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of learners achieved a positive career outcome

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Dieser Kurs ist Teil der Spezialisierung Spezialisierung „Clinical Trials: Good Clinical Practice “

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In diesem Kurs gibt es 3 Module

Welcome to 'Introduction to Good Clinical Practice'! This course is designed to introduce you to the basic principles and practices of Good Clinical Practice (GCP), which are essential for conducting clinical trials and ensuring the safety and well-being of human subjects. Whether you are new to the field or seeking to refresh your knowledge, this course and its sequel courses covering the fundamentals of Good Clinical Practice will equip you with the necessary skills and understanding to begin to navigate the complex world of clinical research.

Developed by industry experts, the course offers an introduction to the key concepts, guidelines, and regulatory requirements outlined in the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) GCP guidelines. During this course, you will explore the essential elements of Good Clinical Practice and gain insights into its significance in the global clinical research arena. By the end of the course, you will have a solid understanding of the principles of GCP and its role in ensuring the integrity and reliability of clinical trial data. The course is divided into several modules, each covering specific aspects of GCP. The modules include video lectures and interactive quizzes to reinforce your learning. You can progress through the course at your own pace, allowing you to fit your studies around your existing commitments and responsibilities. We are excited to embark on this learning journey with you as we delve into the world of Good Clinical Practice. Enroll now and start building a strong foundation in clinical research ethics and regulations!

Moduldetails

In Module One you’ll learn the basics of what a clinical trial is. You’ll hear from investigators, patients, and sponsors about the benefits of clinical trials, and you’ll learn about the drug discovery process.

Das ist alles enthalten

7 Videos1 Lektüre3 Aufgaben

7 VideosInsgesamt 21 Minuten

Introduction to Good Clinical Practice2 Minuten
What's a clinical trial?2 Minuten
What are the phases of clinical trials?2 Minuten
Why participate in a clinical trial?1 Minute
A sponsor's view of clinical trials3 Minuten
Drug research and development7 Minuten
Who conducts clinical trials and why?3 Minuten

1 LektüreInsgesamt 3 Minuten

Introduction to our characters3 Minuten

3 AufgabenInsgesamt 40 Minuten

Challenge5 Minuten
Challenge5 Minuten
Module One Graded Assessment30 Minuten

In Module Two we’ll focus on some important rules and regulations. You’ll find out why good clinical practice matters and learn about the history of regulatory frameworks for medical treatment and testing. We’ll also explore some clinical trial definitions, look at informed consent, talk about risk, and discuss data integrity.

Das ist alles enthalten

6 Videos4 Aufgaben

6 VideosInsgesamt 15 Minuten

Definitions of words used in clinical trials2 Minuten
Medical care vs clinical research1 Minute
What are the risks and benefits of clinical trials?2 Minuten
The history of Good Clinical Practice and why it matters5 Minuten
What is informed consent?3 Minuten
Data integrity principles overview1 Minute

4 AufgabenInsgesamt 48 Minuten

Challenge5 Minuten
Challenge8 Minuten
Challenge5 Minuten
Module 2 Graded Assessment30 Minuten

In Module Three we’ll explore how research in clinical trials makes a difference. We’ll also walk you through what medical teams and patients must do to become involved. You’ll learn about the importance of diversity in clinical trials, inclusion and exclusion criteria, and we’ll hear from some patients who’ll tell us how they experienced the trial process.