Internal audits are a fundamental part of implementing, maintaining and improving your quality system which is critical to your business’ success.

Whether you work for a pharmaceutical company complying with “self inspection” requirements of the PIC/S Guide to GMP or a medical device company complying with “internal audit” requirements of ISO 13485, deploying an internal audit program throughout your organisation will help educate personnel, confirm ownership of various quality system elements and ultimately drive continuous improvement and cost reductions.

quality team reviewing documents in an internal audit or self inspection

Internal audits deliver value irrespective of how mature your organisation’s quality system is.

Do you need help optimising and delivering more value from your self inspection / internal audit program? This course can help you achieve your KPIs.


You will learn and practice techniques for preparing audit plans, performing audits, verifying observations and reporting.

  • GxP and Quality Auditing
    • Critical role of quality audit in GMP compliance & improvement
    • Regulatory standards and guidelines for quality auditing
    • GxP requirements for internal audit programs
    • Risk assessment as it applies to quality audit practices
    • Documents, records & data for effective audits
    • GxP audit schedules and the use of risk management in relation to prioritising audits
    • Six fundamental steps of auditing explained in detail (including tips on how to manage & facilitate audits in a constructive manner)

This course is designed for operational personnel (key operators, supervisors and managers) who have a key role in quality systems implementation and will assist them to develop a system of quality audit.

Format and Course Length

The course will be delivered as an online virtual-classroom training session.

Participants will be provided with a PDF of the training material in advance of the training should they wish to print and annotate notes. Participants will be connected to the trainer and other participants via online collaboration tool Zoom with connected video (webcam / screen sharing) and audio (computer audio or phone dial-in). Theory will be delivered by the trainer sharing their screen of the PowerPoint presentation. Facilitated workshops will be run in digital breakout rooms (e.g. a group of 12 might split into 4 breakout rooms each with 3 participants to separately work on a problem). Breakout rooms can call the trainer in for support when required and the trainer can electronically bring everyone back to the main session to debrief when appropriate.

The training is delivered as 2 x half-day sessions over 2 days. Breaks are included.

PDF Certificates will be provided to participants electronically.

What Do I Need?

Participant needs are very basic. You will need a computer or suitable device with a good internet connection. A headset (headphones with microphone) and second monitor/screen are recommended but not required.


Each participant will attend both half-day sessions:

 Sessions  Dates  Times
 Day 1  28th October 2021  1:00pm-5:00pm
 Day 2  29th October 2021  1:00pm-5:00pm

Times are based on Melbourne, Australian Eastern Daylight Time (AEDT) / Coordinated Universal Time (UTC) +11:00.

Fee and Discount
  • AUD $600 (excluding GST) per participant
    • A 10% discount applies for 3 or more participants from the same company

New Session Dates To Be Advised

Contact us for clarification or to discuss your interest in public or private delivery of this course .

Refer to the Terms and Conditions

Jacqueline Berry Circle Gradient Grey BG 300x300

Proposed Trainer

Jacqueline Berry

Jacqueline has over 20 years of experience in the Pharmaceutical industry with specific experience in Quality Management Systems development and maintenance. In that time, Jacqueline has conducted numerous GxP/Quality Audits; conducted gap assessments and delivered training programs to organisations around Australia. In her current role at SeerPharma, Jacqueline leads the lecturing effort of SeerPharma’s Postgraduate GMP Program at the University of Technology Sydney and is actively involved in the development and delivery of this program.