Good Laboratory Practice Training

Course code: GLP01

Overview

This GLP course is updated regularly to provide participants with current GLP trends and information.

This course is designed for staff working in the early phase drug development and commercial operations.

As the FDA states;

"Each individual engaged in the conduct of or responsible for the supervision of a nonclinical laboratory study shall have education, training, and experience, or combination thereof, to enable that individual to perform the assigned functions."

Course Duration & Location

One day, on your site or at an offsite location.

PharmOut's training courses can be delivered anywhere in the world. If your site is not in a city we have an office in then we ask you to cover the travel costs from our nearest office. You'll save the costs associated with your staff travelling to be trained, so it becomes cost effective if you have several people needing training.

Pricing

Indicative pricing is US$490 per person, with discounts available when more than 10 people attend the same course.

What you will learn

Upon completion of this course participants will;

• understand the basics of GLP and basic good documentation practice
• be able to adopt GLP requirements into your daily work tasks and non-clinical projects
• have a relevant working knowledge of the ISO 17025 and OECD GLP principles
• know the roles and functions of key personnel within a GLP study
• be able to develop GLP compliant documentation
• understand the Quality Assurance Unit and its role in GLP management responsibilities in a GLP context

Course materials

Participants will receive a copy of the presentation(s), relevant notes and workshop materials.

A certificate of completion will be issued to participants who successfully complete the assessment.

Assessment

A written assessment is conducted at the end of the course.

Course Format

The course is a combination of lecture-style learning and active workshops with participants working in small groups on assigned tasks.

Who should attend?

• Quality Assurance / Quality Control personnel
• Laboratory personnel
• People new to the GxP regulated industries

More information

If you would like a quote or would need to ask questions, please contact us.