With special guest Dan Mans
From Australian FIH to global regulatory approvals
Summarizing the Tendyne AUS Experience
Mobius + Tiller Design webinar Gain valuable insights about medical device design and development from one of Australia's most seasoned industrial designers, Robert Tiller. Robert, Founder of Tiller Design and Head of Design at EM Vision Medical Devices is Suzanne's special guest for this discussion. Robert Tiller Head of Design - ASX-EMV. Led the translation of core technology from Uni of QLD into a POC device and first clinical trial device. Founder - Tiller Design. A Multi disciplinary Design Firm
The top 5 features to look for in today’s EDC’s and why they matter! - Real-time Data Monitoring - eModule Availability - Easy and Clean Data Extraction - Integrated Medical Coding - Data Security and Privacy Elena Elefantis - Clinical Data Manager & Clinical Research Associate Thomas Choat - Clinical Data Manager
Today we are joined by Michelle Catto Associate patent attorney from FB Rice mcatto@fbrice.com.au Outline - Introduction to intellectual property - Intellectual property issues in clinical trials - Best practices for managing IP in clinical trials
Today we are fortunate to be joined by Josh Meyer, CEO of Avatar Brokers Pty Ltd
Topics discussed
All about the Australian Research & Development tax incentive program.
Today we are fortunate to be joined by Blair Lucas from Acclime.
Topics
Welcome to Mobius Medical’s September webinar!
In today’s session we will be focusing on how clinical trials are approved in New Zealand and the various regulatory bodies you need to consult with prior to starting your project.
Clinical Trial Start up
The Clinical Trial landscape in ANZ in brief
How to achieve site activation in under 3 months
Recruitment
Tips for planning, and executing recruitment goals
Close-out
Integration into the CRO industry from academia, research and the bedside
Pathways from Academia and Research
Pathways from Bedside
Pathways from Clinical Site
CRO Life
Virtues of Going Virtual
Reduce the burden on participants
Reduce the burden on the healthcare system
Greater oversight of the study
Deeper understanding of study performance and user experience
Improve clinical trial recruitment!