COURSE ID 545

Good Laboratory Practices (GLP)

AVAILABLE On-demand
8 Hours

On-Demand

Offering Price
$ 1300
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Team Training

When you need on-site attention, we’re not just here to help, we’re there to help—right by your side.

Individual courses are remarkably effective. But sometimes when you have a specific need, it helps to have expert guidance right in the room with you and your team.

In that case, we’re happy to design a custom training for your entire team, whether online—or on-site.

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Remember – at checkout you can choose to take this course On-demand. We offer a 10% group discount when you register 2 of more attendees (up to 10). Contact us for larger groups.

Benjamin Franklin famously said:
Tell me and I forget, teach me and I may remember, involve me and I learn. This course has been entirely redesigned with this cogent observation in mind so that each person can get involved in problem-solving and thus learn about Good Laboratory Practice (GLP) Regulations.

Overall, the main intent of this course is to review all the requirements of Good Laboratory Practices (GLP) regulations for facilities engaged in regulated Safety Testing. The learning initiative is achieved through a mixture of short lectures, illustrative answers to FAQs, and collective problem-solving workshops. The aim is to ensure that each participant is personally faced with real-life situations for which GLP-compliant solutions have to be found.

You will be challenged with the issues of data integrity and the problems of study reconstruction, as well as asked to give your own reactions to real-life situations and to solve the issues arising in a way compliant with the regulations. Involving you in the GLP decision-making processes means that you will learn and understand rather than just receive information as you would from a standard course.

This 8-hour accredited course will concentrate on existing FDA and OECD Good Laboratory Practices and their application to the workplace including recent developments such as multi-site and short-term studies. Lectures will address how to prepare and react to inspections.

This intensive, practical course will be of value to those professionals in the pharmaceutical, medical device and related industries who are responsible for or involved in any interaction with suppliers, including:

– Scientists
– Regulatory/Compliance Personnel
– Quality Assurance Staff
– Those newly assigned GLP Responsibilities
– More experienced personnel needing to update their knowledge

course instructor

David Long
Long and Associates International Consulting Ltd.

David Long’s Courses
David Long worked for Rhône Poulenc Health Division (now Sanofi-Aventis) in Quality Assurance (QA) for over twenty years where he gained considerable experience in all three Good Practice disciplines, GLP, GCP and GMP. When he left Rhône-Poulenc he was Senior Director R&D worldwide for Quality and for Process Improvement. Mr. Long has since worked for CHIMEX, a manufacturing subsidiary of the L'Oréal group and now runs his own consultancy company. David Long has always shown a keen interest in promoting professional QA activities. He was a founding member and President of the French QA Society and a founding member and President of the European QA Federation. He was also the founder and Chief Editor of the Quality Assurance Journal, an international scientific journal specifically addressing subjects of interest to R&D and QA personnel. He has lectured and trained widely and has been an active participant in developing training in Good Practices and QA, working with a number of international groups including the OECD and the WHO. His latest contribution through the WHO has been in the co-authoring of a set of guidelines for research performed upstream of the regulatory scene, called Quality Practices in Basic Biomedical Research.