Translating Clinical Research Into Clinical Practice
We are dedicated to providing high quality clinical research services & consultancy to support you
in transforming medicine
About ElliClinical
Our Mission
At ElliClinical, our mission is to work alongside you to advance clinical research through provision of expert clinical research services.
We are different by design.
Our Clinical Research Services
Preclinical and Clinical Operations
Comprehensive preclinical support along with clinical trial management and product translation services:
- Local director or sponsor support
- Biotech and Medtech
- Preclinical consulting, documentation support and regulatory alignment
- Product development and clinical strategy consulting
- Project management of Pilot/Phase 1 to Post-market studies
- Compliance monitoring
- Safety reporting and management
- Good clinical practice (GCP) training
Site and Field Support
Clinical specialists who are certified in good clinical practice to support site investigators or sponsor teams.
Experts in Clinical Trials
Experienced and clinically trained to bring a diverse range of skills and expertise to every project.
Whether it is medtech or biotech, we support sponsors, CROs and site investigators in conducting the studies.
We also have a special interest in software as a medical device (SaMD) and use of AI tools
Our Network
Collaborations with the best in the industry.
We work with a large network of vendors to deliver high quality and compliant clinical trials.
We bring key opinion leaders to you.
Running a Trial in Australia
Australia offers world-class clinical trial and R&D services, as demonstrated through:
* Efficient trial start-up and regulatory timelines.
* Expertise in early phase trials.
* Provision of high-quality data that aligns with global regulatory standards.
* Cost effectiveness and up to 43.5% R&D tax rebate for eligible entities.
* More than 6000 highly skilled professional services.
* More than 200 clinical trial sites across the country and access to subject matter experts.
Global Populations and Markets
Whether you plan on running clinical trials in Asia-Pacific, US or EU, a strategic approach is required to address regional regulatory frameworks, patient recruitment and market access considerations.
We can assist you in navigating these requirements while bringing operational efficiency across diverse healthcare ecosystems.
Good Clinical Practice Trained
Enhancing success in innovative biotech and medtech
Contact Us
Want to learn what makes us different?
Brisbane, Queensland, Australia
Frequently Asked Questions
We are committed to providing accelerated pathways to achieve optimal preclinical development studies right through to rapid clinical study start-up and management.
Our collaboration and partnership with other industry leaders allows us to achieve the best outcome for you.
We offer a comprehensive suite of services ranging from; preclinical and clinical consulting, clinical trial directorship, project management, monitoring, product development support and clinical site support.
We believe in science so we support all groups ranging from investigator-led studies to large companies.
We have expertise in many areas of medical research, including medical devices, pharmaceuticals, vaccines, gene therapies and more.
We specialize in first in human studies for novel products.
We are your clinical research partner.
We have expertise in running clinical trials in Asia-Pacific, United States and Europe.
We will work alongside you or a local partnering CRO to ensure local regulatory compliance.
We know start start ups have limited resources which is why we believe in assisting across multiple areas of need. We stay with you through the journey.
We help start ups navigate the complexities of product development by designing efficient trial strategies, ensuring regulatory compliance, working with local subject matter experts, and focusing on accelerating market approval and patient access.
Yes we can.
We have a special interest in SaMD and can appreciate the unique requirements these medical devices have with regards to clinical validation and regulatory requirements.
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