Quality Risk Management (QRM) was introduced to the GMPs in 2009 and should now be an integrated part of your daily pharmaceutical manufacturing operations…but is it? Do you know which QRM tool to use in different situations? Are you satisfied that the time and effort in conducting risk assessments is adding real value to your business? Are you confident that your risk evaluation has identified the appropriate level of manufacturing controls? This training can help by providing you with relevant knowledge and skills to effectively participate in process risk assessments. You will gain a general understanding of manufacturing processes and how they are controlled, as well as an understanding of the Risk Assessment Process to ensure you have a basis from which to conduct a structured risk evaluation.

ASEAN Pharmaceutical Bottle Line

  • Manufacturing considerations: what can go wrong, complex processes and systems
  • Overview of the Quality Risk Management Process
  • GMP requirements for risk assessment
  • The Quality Risk Management Toolbox: what to use and when
  • Conducting Process Risk Assessments, considering:
    • Preliminary Hazard Analysis (PHA)
    • Hazard Analysis and Critical Control Points (HACCP)
    • Failure Mode and Effects Analysis (FMEA)

This course is designed for both personnel new to process risk assessment as well as more experienced QRM practitioners. You will benefit from this course if you have a simple interest in or have any level of responsibility for risk assessments of manufacturing processes.

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 will be delivered as 2 half-day sessions with breaks.

PDF Certificates will be provided to participants electronically.

 Sessions  Dates  Times
 Half-Day 1  20 April 2021  8:45am join for 9:00am-12:30pm
 Half-Day 2  21 April 2021  8:45am join for 9:00am-12:30pm

Times are based on Singapore time (SGT): UTC +8:00

Participants to join at 8:45am in advance of a 9:00am start to address any technical issues.

  • SGD $650 (excluding tax) per participant
    • A 10% discount applies to 3 or more participants from the same company
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.

Course Registration and Payment

Please contact Shanice Pan at shanice@seerpharma.com (DID: +65 6914 9068)

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

Refer to the Terms and Conditions