NSW Health
Commercialisation
Training Program

This seminar is for anyone who wants to develop a high-level understanding of the regulatory landscape and pathways for NSW-based innovations that have a global view.

During this seminar, you’ll hear from experts about the key details you need to understand about regulatory affairs in Australia, the United States, Canada, the United Kingdom, and Europe. 

You'll also learn about,

• - Correspondence and implications of clinical trials, regulatory affairs, and quality management systems.
• - Regulatory bodies, pathways, and timelines in Australia, the US, Canada, the UK, and Europe Therapeutics & Pharmaceuticals.
  
• - Regulation including frameworks and classifications of medicines, managing the planning process, developing with the outcome in mind, product development, sale/supply, and post-marketing.
  - Medical Device, Diagnostics, and Software as a Medical Device Regulation in Australia: Regulations, definitions, and classification, Regulatory submissions, and Quality Management Systems

This seminar is for anyone who wants to understand what the healthcare system looks like today and how the different pieces work and collaborate. During this seminar, you’ll hear from different parts of the healthcare system on how they work, who the key stakeholders are, what the procurement and decision making process looks like, and what it takes to succeed.

• - What different components make up the NSW and Australian health system and the role and structure of these.
• - Key terminology to understand
• - Who is involved in funding healthcare innovations
• - Quality, safety, infrastructure, and the workforce in health.
• - How to find the key decision makers and navigate the procurement processes and purchasing behaviours for key health stakeholders for in-hospital and out-of-hospital public services, the private system, the primary healthcare system (general practitioners), allied health, aged care, and the NDIS.