Clinical Translational Catalyst
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What Is CTC?
Catalysing clinical translation to bring innovative, life-changing therapies and technologies to patients, the Clinical Translational Catalyst (CTC) is a highly specialized platform to provide all-round support to biomedical companies in pre-clinical and early clinical stage.
Under this programme, Financial Support will be provided to biomedical companies of HKSTP with highly promising pre-clinical/ clinical projects. In addition, a Professional Network of key stakeholders are engaged by CTC team to work together with your product development towards attaining regulatory approvals, conducting clinical trials and achieving commercialisation. To transform Hong Kong as a leading clinical translational research hub within the region, an overarching Clinical Translational Consortium has been established.
Financial Support
Regulatory Affairs Funding Scheme
Subsidise 50% of expenditure for preclinical/nonclinical activities for
- Therapeutics, up to HK$4 million
- Class III medical devices, up to HK$2.5 million
- De novo medical devices, up to HK$1 million
- Class II medical devices, up to HK$0.5 million
Clinical Trial Funding Scheme
Subsidise 50% of expenditure for clinical trials for therapeutics and medical devices, up to HK$8 million.
Are You Eligible To Apply For CTC Financial Support?
You are eligible to apply for this highly selective programme if:
- You are an existing HKSTP tenant*
- You have at least 3 full-time staffs working at your leased premises at Hong Kong Science Park
- You will remain as HKSTP tenant for the entire term of the funding scheme
- The project coordinator and project team are full-time employees of your company at HKSTP
* Companies which are not HKSTP tenants should first apply for tenancy
EnquiryProfessional Network
Providing access to scientific, clinical, technical and regulatory experts, as well as commercial partners, our Professional Network Support is available for catalysing the translation of novel and breakthrough biomedical technologies from pre-clinical to clinical development stage.
Support available via the Professional Network
- Learn about the latest regulatory updates via webinars and workshops
- Connect with experts to understand the regulatory approval and clinical trial processes
- Establish your network of principal investigators, technical experts and commercial partners (e.g. CROs, CDMOs and CMOs)
ASK CTC! is a specialized HELPDESK designed to help biomedical companies to kick-start their translational journey towards regulatory submissions and clinical trials.
Partners In Our Professional Network
Clinical Translational Consortium
On behalf of the Hong Kong clinical research community, the Clinical Translational Consortium is established to provide strategic thought and SUPPORT policy development for strengthening the clinical translation research environment.
Vision
Establish Hong Kong as a leading clinical trial hub within the region.
Mission
Strengthen Hong Kong’s clinical trial environment by leveraging the combined strengths of Hong Kong and the rest of the Greater Bay Area.
Goals
- Provide strategic thoughts and implement ideas to strengthen local clinical research environment and enhance the competitiveness of Hong Kong as a clinical trial hub
- Build an information platform and provide the industry, academic, and public with compendious information about clinical trials in Hong Kong
- Promote Hong Kong as a clinical trial hub and attract national and overseas biomedical companies landing in Hong Kong
Our Consortium Members
Our Work
Hong Kong Science & Technology Parks Corporation supported Our Hong Kong Foundation in the release of the research report - “Developing Hong Kong into Asia’s Leading Clinical Innovation Hub”, on the 30 November 2023. Drawing upon insights from 250+ stakeholders, the report identifies clinical research as a strategic pillar of Hong Kong’s Innovation & Technology Development and advocates for the Government to strengthen its role in facilitating clinical research through a Clinical Research Institute, establish a primary review authority for drug registration and to build a comprehensive talent development strategy. The research report had been submitted to the Health Bureau, the Innovation, Technology and Industry Bureau and 2023 Policy Address Public Consultation.
Double click to read the e-version of the research report