Print...

Good
Clinical Practice in Clinical Research (non-drug trials)

12th September
2018

Edinburgh WTCRF, Education
Programme

This is
to certify that

Heather
Anderson

Attended
the above session

Course Objectives

Understand the 13 principles of Good Clinical Practice, and who is
responsible for implementing the principles & concept of research
‘sponsor'

Identify when specific regulatory requirements apply

Understand what is meant by ‘risk assessment’ and the common threats
associated with research involving humans

Understand the quality of research protocols and the quality of research
data is assured, and what is meant by ‘quality’ and ‘quality assurance’

Aware of the NHS / University governance processes, including arrangements
for indemnity - Honorary contracts and research passports

Consider the training needs for yourself and those who you have management
or supervisory responsibility for

Reference: 63256