Details
Organisation Name: UniSC Clinical Trials – Morayfield
HHS: N/A
Services Offered: Clinical trials site,Trial Patient Recruitment
Website Address: www.unisc.edu.au/community/unisc-clinical-trials-clinical-trial-site-ne…
Contact: Tom Nott- BDTrials@usc.edu.au
Other Affiliated Research Sites: Sites across South East Queensland, UniSC Clinical Trials is conveniently located in Maroochydore, Sippy Downs, Morayfield, Birtinya, Brisbane, and Meadowbrook.
Location
-27.097942252037416, 152.95069818326255
Is your Facility able to initiate study activities prior to Ethics Committee protocol approval?
No
Site Overview
Our Morayfield clinic, located within Health Hub Morayfield, is dedicated to early phase clinical research, including first-in-human studies and trials requiring overnight stays. With 20 beds, the facility is designed to provide a comfortable experience for participants while supporting the delivery of high-quality clinical research.
HREC
- HREC Committee Name: Bellberry Limited
- Meeting frequency: Weekly
- Types of HREC (IRB/ERB/ETHICS) Committee that are used: Central Acting as Local
- Mandate distribution of safety: Yes
- Meeting frequency: Weekly
- Types of HREC (IRB/ERB/ETHICS) Committee that are used: Central Acting as Local
- Mandate distribution of safety: Yes
Facility staffing and training
- Handling Investigational Product: Yes
- Training program for the research staff: Yes
- IATA Training: Yes
- Include GCP: Yes
- Facility written SOP during transportation to satellite site: Yes
- Training program for the research staff: Yes
- IATA Training: Yes
- Include GCP: Yes
- Facility written SOP during transportation to satellite site: Yes
Licenses to receive, store, dispense and return controlled substances
- Required Licenses or Registrations: Yes
Equipment
- Investigational Product: Vertical laminar flow hood (chemo/hazardous drugs)
- Centrifuge: Yes
- Refrigerated Centrifuge: Yes
- Centrifuge: Yes
- Refrigerated Centrifuge: Yes
Patient Records
- Record Archiving (on-site): No
- EMR/EHR systems: No
- EMR/EHR systems: No
Investigational product storage Capabilities
-Refrigerator (2 to 8 Degrees C): Yes
- Freezer (-20 to -30 Degrees C): Yes
- Investigational Freezer (-70 to -80 Degrees C): No
- Investigational Freezer (Liquid Nitrogen -135 Degrees C): No
- Does this equipment have back-up power? Yes
- Does this equipment provide Min/Max Temperature Monitoring? Yes
- Do you have the ability to generate a temperature monitoring log for this equipment? Yes
- Does this equipment have a temperature alarm? Yes
- Do you have an SOP which supports calibration of this equipment? Yes
- Freezer (-20 to -30 Degrees C): Yes
- Investigational Freezer (-70 to -80 Degrees C): No
- Investigational Freezer (Liquid Nitrogen -135 Degrees C): No
- Does this equipment have back-up power? Yes
- Does this equipment provide Min/Max Temperature Monitoring? Yes
- Do you have the ability to generate a temperature monitoring log for this equipment? Yes
- Does this equipment have a temperature alarm? Yes
- Do you have an SOP which supports calibration of this equipment? Yes
Specialty Research Area
Cardiovascular Diseases
Digestive System Diseases
Endocrine System Diseases
Eye Diseases
Female Urogenital Diseases and Pregnancy Complications
Hemic and Lymphatic Diseases
Immune System Diseases
Male Urogenital Diseases
Mental Disorders
Musculoskeletal Diseases
Nervous System Diseases
Nutritional and Metabolic Diseases
Otorhinolaryngologic Diseases
Parasitic Diseases
Pathological Conditions
Respiratory Tract Diseases
Signs and Symptoms
Skin and Connective Tissue Diseases
Stomatognathic Diseases
Virus Diseases
Wounds and Injuries
Study Types
Industry
Source Document Types
Electronic
Has your Clinical Trials Site or Service been audited by:
Other
Sponsor
Average time to start study (in calendar days)
30-60
How long prior to HREC meeting does the application need to be submitted?
2 weeks
Does the HREC committee require contract /budget approval prior to release final approval documents?
No
Does your Facility support in-patient admissions?
Yes
PK & PD specimens
Yes
Study Phase Capability
Device Pilot
Device Pivotal
Device Post Approval
Phase I
Phase II
Phase III
Phase IV
Type of Diagnostic Equipment
CT Scan Computerized Tomography Scan
DXA Dual-Energy X-ray Absorptiometry or Bone Densitometry
ECG/EKG Electrocardiogram
FLRO Fluoroscopy
MAMMO Mammography
MRA Magnetic Resonance Angiography
MRI Magnetic Resonance Imaging
MRS Magnetic Resonance Spectroscopy
Other
Perfusion CT
PET Positron Emission Tomography Scan
SPECT
Thyroid scan
X-Ray
Patient Population
Adults - Ages 18-64
Geriatrics 65 and onwards