An Introduction to Good Clinical Practices (cGCP) – Part 1
Description: Good Clinical Practice (GCP) is an international ethical and scientific quality standard provided...
Certified Online Course
2-Minute Guide to Clinical Trial Investigators
Qualifications The Investigator should be qualified by education, training, and experience to assume responsibility...
Key Principles of Good Clinical Practice (GCP) Part 2
The final six principles of GCP are: Research personnel qualification Voluntary informed consent Data...
Key Principles of Good Clinical Practice (GCP) Part 1
There are 13 key principles of Good Clinical Practice (GCP). The first seven are:...
GCP | The Belmont Report Explained
In 1979, the Belmont Report was issued by the National Commission for Protection of...
Major Responsibilities of the Institutional Review Board (IRB)
The major responsibilities of Institutional Review Board (IRB) / Independent Ethics Committee (IEC) include:...
The Informed Consent Process for Clinical Trials [Video]
Informed consent is more than just a signature on a form, it is a...
The Meaning of Informed Consent for Clinical Trials [Video]
Informed consent is a written agreement by which a subject voluntarily confirms his or...
What is an Institutional Review Board (IRB/IEC)? [Video]
An Institutional Review Board (IRB), also known as an Independent Ethics Committee (IEC), is...
What are Good Clinical Practices (cGCP) [Video]
Good Clinical Practice (GCP) is an international ethical and scientific quality standard provided by...
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