STARTUP SUPPORT
Startup Guide
This guideline outlines the key components involved in translating healthcare innovations at HKU from early-stage ideas to real-world impact. While the specific sequence of steps may vary depending on the nature, stage, and needs of your project, the following areas should be considered:
01 Commercialisation 02 IP Protection 03 Venture Building 04 Declaration & Licensing 05 Clinical Development 06 Incubation & Fundraising
Engage with the relevant HKU units early—including the HKU Versitech, HKU Clinical Trials Centre (HKU-CTC), HKU TEC, and other partners—to reduce risk, accelerate development, and maximise the impact of your work.
01 Commercialisation Assessment
- Analyse the market to pinpoint opportunities in healthcare and outline commercialisation strategies.
- Identify regulatory pathways at an early stage.
- Seek advice from us and the HKU Versitech to evaluate prospects and feasibility.
02 IP Protection
- Work with the IP Management Team to plan and file patents, ensuring protection is in place before any public disclosure.
03 Venture Building
- Begin assembling your team as early as possible.
- Consider reaching out to TEC, which offers talent-matching support partnering with CEDARS and advice on start-up essentials such as market validation, business planning, and shareholding structure through mentors and Service Partners.
04 Declaration & Licensing
- Follow the instructions to make a Declaration of Interests via the HKU Portal.
- Secure a licence from HKU Versitech Limited if you intend to use HKU-owned IP; such agreements may be structured around clinical milestones.
- For standard templates of research-related agreements (e.g., licensing agreements, material transfer agreements, collaboration agreements), refer to the HKU RISE Research Agreement Template page.
05 Clinical Development
Many projects require clinical data to support validation, safety, efficacy, and regulatory approval.
- Work with the HKU Clinical Trials Centre (HKU-CTC) for the design, management, and conduct of studies, from pre-clinical stages through Phases 1–4.
Prepare a study protocol early and obtain:
1) Ethics approval from the HKU/HA Hong Kong West Cluster Institutional Review Board (IRB)
2) Regulatory approval from the Hong Kong Department of Health
- Seek advice from us and HKU-CTC on compliance, submissions, ongoing IRB reporting, and data privacy/biosafety. Early consultation is recommended to reduce risk and speed up development.
06 Incubation & Fundraising
- Participate in innovation competitions, e.g. HKUMedXelerate, to gain training, mentorship, and professional networks.
- Consider funding opportunities offered by HKU, Innovation and Technology Commission (ITC) and health-focused incubators (e.g. the Hong Kong Science Park Biomedical Cluster).
