Frequently Asked Questions
General FAQs
Cureos is an Australian clinical research network specialising in ophthalmology and retinal diseases. We work collaboratively with clinicians, industry partners, and research sites to conduct high-quality clinical trials, provide site management services, and support medical research initiatives.
Cureos provides:
- Clinical trial management
- Site management services
- Patient recruitment support
- Medical writing and publication support
- Research network collaboration
- Training and mentoring for research sites
Our goal is to improve patient outcomes through innovative clinical research.
Cureos currently supports research sites across New South Wales, Queensland, Victoria, South Australia, and Tasmania, with plans for further expansion throughout Australia.
Health Care Providers FAQs
Please refer potentially eligible patients to Cureos for assessment. Our team will review the patient’s suitability and facilitate referral to an appropriate clinical trial site.
By referring patients to clinical trials, you may help them:
- Access emerging therapies
- Receive additional monitoring and imaging
- Contribute to future advances in eye care
- Explore treatment opportunities when standard options may be limited
Yes. Cureos provides comprehensive support for practices interested in establishing or expanding clinical research activities, including:
- Study feasibility assessments
- Ethics submissions
- Site start-up support
- Research coordinator assistance
- Training and mentoring
- Ongoing operational support
These services can be tailored to the needs of your practice.
Absolutely. Cureos can help with identifying suitable studies while providing the support required to successfully complete clinical trials and/or research programs.
Research Partners and Sponsors FAQs
A Site Management Organisation (SMO) provides operational, regulatory, and administrative support to research sites conducting clinical trials. This helps investigators focus on patient care while ensuring studies are conducted efficiently and compliantly.
Our services include:
- Site start-up and activation
- Ethics and governance submissions
- Budget and contract support
- Patient recruitment strategies
- Research coordination
- Regulatory compliance support
- Monitoring and ongoing site management
Yes. Through our clinical research network, we collaborate with clinicians and researchers to develop and conduct investigator-initiated studies addressing important clinical questions.
Yes. Our team provides medical writing support for research protocols, manuscripts, conference abstracts, posters, and scientific publications.