Annual cGXP Update

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Who Should Attend: This is a course designed for any person working in an FDA-regulated bio/pharmaceutical company. This includes all departments (manufacturing, analytical, quality, warehouse/shipping, development teams) and all levels from your most junior to the most senior staff.

Scroll down to learn more about the course. Sign up and receive a link to the for the recorded session and listen at your convenience. When you are ready, click on the “Register Now” button to sign up for the course.

The course includes a quiz which tracks your attendance and attention. From this you can be issued a GXP Update Training Course certification with the date of your training.

This 120-minute course is only $630! (+ $50.00 for training certification) Great group discounts are available.

FREE EXCERPT! Want a preview of the Annual GXP Update Course?
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Annual cGXP Update Course Outline

  • Instructor: Dr. Laureen Little
  • Format: On-demand recording available soon.
  • Content:
    ● US Regulatory History
    ● Overview of GMP, GTP, and QSR Regulations
    ● This Year’s Inspection Results
    ● This Year’s Case Study
    ● Top Inspection Observations
    ● Records and Reports Rules and Case Study
    ● Corrective and Preventative Actions
    ● Data Integrity and Documentation
    ● Electronic Documentation
    ● Failure Investigations
    ● Organization and Personnel
    —○ Training and Qualifications
    ● Design and Construction
    ● Cleaning/Gowning/Aseptic Issues
    ● An FDA Auditor’s Tale
    ● The Crystal Ball

COPYRIGHT: U.S. Copyright Law protects the program you are about to attend from unauthorized duplication. Multiple participants are not authorized to share access provided to a single registrant.  For each individual who attends, a single dedicated seat license must be purchased, or a group rate must have been previously arranged with FasTrain. FasTrain reserves the right, at its discretion, to cancel or interrupt access to a web-based training class without notice, or to invoice and collect the group rate payment for the class from the single registrant if this requirement has been violated.