Selected Presentations from Pharma & Device Forum 2025
Not all presentations from the Pharma & Device Forum are able to be shared. Below are those where permission has been granted by the speaker.
Day 1
Plenary
Brisbane Room
Perth Room
- Packaging Reform and APCO’s 2030 Strategy
Sandra Dal Maso - Laboratory Business Sustainability: Ensuring Compliance and Customer Confidence through Automation
Helen Evans-Lemmo - Forever Chemicals – Imagine Not Being Able to Use PVDF tomorrow
Michael Schafferius - Isolators vs. Open Cleanrooms: Designing the Future
Ian Henton-Smith
Sydney Room
- The Ins and Outs of Implementing USP Chapter <86> for Bacterial Endotoxin Testing
Alan Hoffmeister - Contamination Control Strategy – Tips for Ongoing Compliance
Ashley Isbel - Characteristics and Challenges of Disinfectant Residues on Environmental Surfaces
David Nobile - A GMP-compliant approach to in-process contamination control and sterility release testing using Celsis® Rapid Microbial Detection platform
Yong Jian Lee, PhD
Day 2
Brisbane Room
- From Research to Revenue – R&D Tax Incentives and Grants Available to Companies
Rosie Silk, Rita Choureri - Therapeutic product development with the goal of being GMP ready
Garima Sharma, PhD - Influencing Top Management for Compliance – How to Talk to Senior Leaders and Get Results
Kathy Walsh - Managing product and process specifications throughout the drug development lifecycle seamlessly
Jofer Princesa - US FDA 483 – Trends and citations relating to Computerised Systems
Trevor Schoerie - Ensuring Compliance and Innovation in a Digital World
Matt Schoerie - GAMP®5, Successes, Opportunities, and Challenges
Siôn Wyn
Perth Room
- Medical Device Regulations on the Move: What’s Changing & How to Adapt
Anne Saletti-Hayes - Boosting Local MedTech: Connecting Manufacturers to Health Procurement
Craig Neylon - Remote Healthcare Revolution (Medical Devices)
John Montalto - Crossing the Rubicon. What to do when oral dose minimisation is no longer effective
Paul Wynne - Medical device manufacturing in Australia
Tom Stray - Device Vigilance – Today and Tomorrow
Carl Bufe - Understanding HBEL & PDE Limits: Cleaning Validation Hurdles in Share Facilities
Luke Philp
Sydney Room
- Background to Radiopharmaceuticals
Nic van der Nol, John Young - Radiopharmaceutical Facility Design
Nic van der Nol - BSL-3 Airborne Surface Disinfection strategy: selection of a new provider for safe and efficient disinfection, cycle development and performance qualification with spores and viruses (Case Study)
Charlotte Gourraud - TM@TRI – Challenges, capabilities, and offerings of a new State-of-the-art biomedical hub
Arman Ergenekon - Successful tips when planning large scale validation program
Shane Bourne - Sterile Success: Achieving Compliance and Efficiency in Aseptic Process Simulations
Kara O’Connor - The Closed Processing Advantage
Andrew Diamond
