Details
- Organisation Name: Royal Brisbane and Women's Hospital- Cancer Care Services
- HHS: Metro North
- Services Offered: Clinical trials site; Investigator Initiated Trials; Trial Patient Recruitment; Treatment of patients; Completion of study documentation as per ICH GCP and contract
- Website Address: www.metronorth.health.qld.gov.au/research
- Contact: Ms Amy Ives- amy.ives@health.qld.gov.au
- Other Affiliated Research Sites: The Prince Charles Hospital
Location
-27.446583 - 153.027796
Initiating study activities approval
No
Review required
2 weeks
Site Overview
The RBWH is a tertiary referral teaching hospital; providing services to patients throughout the State; Northern New South Wales and the Northern Territory; incorporating all major health specialties including medicine; surgery; psychiatry; oncology; women's and newborn services; trauma services and more than 30 subspecialties.
HREC
- HREC Committee Name: MNHA and MNHB
- Meeting frequency: Monthly
- Types of HREC (IRB/ERB/ETHICS) Committee that are used: Central Acting as Local
- Mandate distribution of safety: Yes
- Meeting frequency: Monthly
- 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
- Include GCP: Yes
- Facility written sop during transportation to satellite site: Yes
- Training program for the research staff: 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
- Does the Facility have the ability to handle radio-labelled Investigational Products? Yes
- Does the Facility have the ability to handle radio-labelled Investigational Products? Yes
Equipment
- Investigational Product: Horizontal laminar flow hood (non-hazardous drug preparation)
- Centrifuge: Yes
- Refrigerated Centrifuge: Yes
- Centrifuge: Yes
- Refrigerated Centrifuge: Yes
Patient Records
- Record Archiving: Yes
- EMR/EHR systems: In-house system
- Has your Clinical Trial Site or Service been accredited? Yes
- Audit Type: Other
- EMR/EHR systems: In-house system
- Has your Clinical Trial Site or Service been accredited? Yes
- Audit Type: Other
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): Yes
- 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): Yes
- 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
Basal Cell Carcinoma
Bladder Cancer
Bone Cancer
Brain Cancer
Breast Cancer
Cervical Cancer
Colorectal
Colorectal Cancer
Gastro Intestinal Solid Tumours
Gastroenterology
Gynaecology
Head and Neck
Head and Neck Cancer
Hepatocellular Carcinoma
Hereditary Angioedema
HR Prostate Cancer
Islet Cell Tumours
Liver Cancer
Lung
Lung Cancer
Malignant Pleural Mesothelioma
Melanoma
Neoplasms
Neuroma
Non-Small Cell Lung Cancer
Ovarian
Ovarian Epithelial Carcinoma
Pancreatic
Pancreatic Cancer
Prostate
Prostate Cancer
Renal
Urology
Study Types
Academic
Industry
Investigator
Source Document Types
Paper and Electronic
Average time to start study (in calendar days)
Greater than 120
How long prior to HREC meeting does the application need to be submitted?
2 weeks
Support in-patient admissions
Yes
PK & PD specimens
Yes
Study Phase Capability
Phase I
Phase II
Phase III
Phase IV
Type of Diagnostic Equipment
Other
Patient Population
Adults 18 and onwards