Momentum Clinical Research-Taringa | Clinical Trials Queensland

More Information

Details

Organisation Name: Momentum Clinical Research
HHS: N/A
Services Offered: Early Phase, Clinical trials site, GP trials, Trial Patient Recruitment, Treatment of patients, Completion of study documentation as per ICH GCP and contract
Website Address: www.momentumclinicalresearch.com.au/
Contact: Shawnna Barrett-Feasibility@momentumclinicalresearch.com
Other Affiliated Research Sites: Other Momentum sites at Brisbane, Sydney Melbourne, NZ

Location

-27.489811899907398, 152.98142737930692

Is your Facility able to initiate study activities prior to Ethics Committee protocol approval?

Yes

How long before Ethics Committee review is the Submission Packet required?

1 Week

HREC

- HREC Committee Name: Bellberry HREC
- 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

Does your Facility have a training program for the research staff?: No, Does the course content include GCP?: Yes, Does the study staff that prepares or transports dangerous goods have training that meets the IATA International Air Transport Association (US) or other countries hazardous training requirements for shipping dangerous goods?: Yes, Is your Facility adequately staffed to support studies with both blinded and unblinded Investigational Product?: Yes

Licenses to receive, store, dispense and return controlled substances

Does the Facility have the required licenses or registrations to receive, store, dispense and return controlled substances as required by local law?: Yes, Does the Facility have the ability to handle radio-labelled Investigational Products?: No

Equipment

-Investigational Product: Extemporaneous Preparation, Horizontal laminar flow hood (non-hazardous drug preparation)
-Centrifuge: Yes,
-Refrigerated Centrifuge: Yes

Patient Records

Patient record archiving on-site?: No,
Electronic Health Records (EHR)/ Electronic Medical Records (EMR)?: Yes

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

Specialty Research Area

Cardiovascular Diseases

Digestive System Diseases

Endocrine System Diseases

Eye Diseases

Male Urogenital Diseases

Musculoskeletal Diseases

Nutritional and Metabolic Diseases

Parasitic Diseases

Pathological Conditions

Respiratory Tract Diseases

Signs and Symptoms

Skin and Connective Tissue Diseases

Virus Diseases

Wounds and Injuries

Study Types

Government

Industry

Investigator

Source Document Types

Electronic

Has your Clinical Trials Site or Service been audited by:

Sponsor

Average time to start study (in calendar days)

61-90

How long prior to HREC meeting does the application need to be submitted?

1 week

Does the HREC committee require contract /budget approval prior to release final approval documents?

Does your Facility support in-patient admissions?

PK & PD specimens

Yes

Study Phase Capability

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

Perfusion CT

PET Positron Emission Tomography Scan

SPECT

Thyroid scan

X-Ray

Patient Population

Adolescents/Adults 16 and onwards

Geriatrics 65 and onwards