RDC Clinical Pty Ltd
Brisbane-based clinical research organisation conducting ethics-approved interventional and post-market clinical studies for complementary medicines, nutraceuticals, functional foods, cosmetics and pharmaceuticals. Services include trial design and conduct (including decentralised/hybrid delivery), participant recruitment and screening, clinical assessments and sample collection, secure electronic data capture and consent, safety monitoring and regulatory/ethics support for studies across Australia.
Industries
N/A
Nr. of Employees
small (1-50)
Services
Protocol development and operational delivery for randomized, blinded and placebo-controlled trials across multiple phases and post-market studies.
End-to-end recruitment workflows including eligibility screening calls, electronic and paper consent processes and participant onboarding.
Conduct of short-term absorption and PK studies with serial sampling, controlled dietary conditions and cannula-based blood draws.
Remote study models including telehealth visits, postal distribution of study products and sample kits, and coordination with local pathology centres.
On-site collection of blood, saliva, urine drug screens, swabs, vital signs and anthropometrics and coordination of imaging and vascular assessments.
Use of accredited software for secure participant data management, electronic consent and e-signature capture, adherence to privacy principles, support for ethics submissions and mandated record retention.
Protocol development and operational delivery for randomized, blinded and placebo-controlled trials across multiple phases and post-market studies.
End-to-end recruitment workflows including eligibility screening calls, electronic and paper consent processes and participant onboarding.
Conduct of short-term absorption and PK studies with serial sampling, controlled dietary conditions and cannula-based blood draws.
Remote study models including telehealth visits, postal distribution of study products and sample kits, and coordination with local pathology centres.
On-site collection of blood, saliva, urine drug screens, swabs, vital signs and anthropometrics and coordination of imaging and vascular assessments.
Use of accredited software for secure participant data management, electronic consent and e-signature capture, adherence to privacy principles, support for ethics submissions and mandated record retention.
Expertise Areas
- Clinical trial management
- Pharmacokinetic and bioavailability studies
- Nutraceutical and complementary medicine research
- Decentralised and hybrid trials
Key Technologies
- Electronic data capture (EDC)
- Electronic consent and e-signature systems with audit trails
- Telehealth and virtual visit platforms
- Randomisation and blinding software
News & Updates
Peer-reviewed clinical trial assessing PEA for acute menstrual pain published in Women & Health.
Randomised, placebo-controlled, double-blind study on PEA effects on microbiome and biochemistry published in Biomedicines.
Clinical assessment of trans-resveratrol oral bioavailability published in Pharmaceutics.
Clinical study showing improved EPA/DHA bioavailability with a self-emulsifying formulation published in European Journal of Nutrition.
Peer-reviewed clinical trial assessing PEA for acute menstrual pain published in Women & Health.
Randomised, placebo-controlled, double-blind study on PEA effects on microbiome and biochemistry published in Biomedicines.
Clinical assessment of trans-resveratrol oral bioavailability published in Pharmaceutics.
Clinical study showing improved EPA/DHA bioavailability with a self-emulsifying formulation published in European Journal of Nutrition.