Live Virtual Learning

DURATION OF COURSE
2 Modules / 3.5 hours

ASSESSMENT
At the end of each module, there will be a short question paper to evaluate and embed learning

CERTIFICATE
Electronic certificate of attendance will be issued to each delegate

Keeping abreast of changes in regulations and expectations is a regulatory requirement and with this course we provide a reminder of the principles of GLP as well as covering what is happening in the GLP world such as new OECD guidance or position papers and the implications and impact on facilities.

Module 1 (2 hours)
This is a general GLP overview of the ten principles of GLP, with focus on the following topics:

  • Roles and responsibilities
  • Study control and data integrity

Module 2 (1.5 hours)
This module covers revised or updated MHRA and OECD guidance and looks at the changes directed by regulatory expectations.

This module also looks at why revisions are necessary as well as key topics where the regulators have identified issues.

This is suitable for anyone involved in regulated pre-clinical research. Specifically, individuals with a working knowledge of GLP including Test Facility Management, Study Directors, QA and study personnel who want to maintain or update their existing knowledge base.

Course Tutors

Tutors are comprised of
Cate Ovington, Principal Associate
Shona Ross, Principal Associate

Course Dates

DATETIME (UCT)SESSIONPRICE
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