See Japanese version here

On the ICH Q9 document slides are available on:

Executive summary for regulators and industry
Background
History
Content
Tools - overall notes
Basic Risk Management Facilitation Methods
Failure Mode Effects (Criticality) Analysis (FMEA & FMECA)
Fault Tree Analysis (FTA)
Hazard Analysis and Critical Control Points (HACCP)
Hazard Operability Analysis (HAZOP)
Preliminary Hazard Analysis (PHA)
Risk Ranking and Filtering
Supporting Statistical Tools
Combination of Tools
Application - overall notes
Integrated Quality Management
Regulatory Operations
Development
Facilities, Equipment and Utilities
Materials Management
Production
Laboratory Control and Stability Studies
Packaging and Labelling
Frequently Asked Questions (Q&A)

 

For creating paper copies of a manual with all slides see the Acrobat (pdf) version:

Executive summary, Background, History, Content and FAQ, Tools / Applications 

Disclaimer: The Q9 briefing pack is offered as a supplementary explanation of the material in ICH Q9. It was prepared by some members of the ICH Q9 EWG for example only. It has not gone through any ICH formal process. It does not represent an official policy/guidance.

Team recruited from the 
Members of the Expert Working Group:

Writers

Name
Organisation
Stephan Ronninger (Chair)
F. Hoffmann-La Roche Ltd
Gregg Claycamp
FDA
Peter Gough
formerly with Eli Lilly Inc.; David Begg Associates
Malcolm Holmes
Glaxosmithkline
Takayoshi Matsumura
Eisai Co. Ltd
Christine Mundkur
Barr Laboratories
Tetsuhito Takarada
Mochida Pharmaceutical Co. Ltd
Hideki Sasaki
Nippon Shinyaku Co. Ltd

 

Reviewer

Name
Organisation
Emer Cooke
EMEA
Diana Dowthwaite
Health Canada
Albinus D'Sa
FDA
Gregg Guyer
Merck& Co. Inc.
David Horowitz
FDA
Yukio Hiyama
MHLW
Georgia Keresty
Centocor
Sabine Kopp
WHO
Urs Kopp
Swissmedic
Jacques Morenas
AFSSAPS
Markus Muller
Swissmedic
Etienne Ouimette
Health Canada
Fred Razzaghi
Consumer Health Care Products Association

Also supported by EFPIA and JPMA ICH Q9 Topic Groups.