Details
- Organisation Name: Paratus Clinical Research
- HHS: N/A
- Services Offered: Clinical trials site, GP trials, Trial Patient Recruitment
- Website Address: https://www.paratusclinical.com/
- Contact: info@paratusclinical.com
- Other Affiliated Research Sites: No
Location
-27.444587830840366, 153.02635457301668
Initiating study activities approval
No
Review required
1 week
Site Overview
Paratus Clinical Pty Ltd has been established to meet an increasing need for local service provision in Australia and New Zealand particularly for early Phase and late Phase Clinical Research. Paratus Clinical provides clinical trial related services to pharmaceutical companies, contract research organizations, biotechnology companies, medical device companies and clinical sites. The site may be a single practice, network of practices, hospital based practice or a similar health care institution that has the infrastructure and staff to meet the requirements of the clinical trial protocol. Paratus Clinical has a qualified and experienced team of clinical research professionals who understand the intricacies of conducting clinical trials. Our experience with the entire process, from feasibility to site closeout, enables us to ensure timely and effective delivery at every stage of a trial. Our dedicated research team is comprised of highly skilled research professionals with many years of experience in all phases of trials and in a myriad of clinical indications.
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: No
- Meeting frequency: Weekly
- Types of HREC (IRB/ERB/ETHICS) Committee that are used: Central Acting as Local
- Mandate distribution of safety: No
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: N/A
- Training program for the research staff: Yes
- Include GCP: Yes
- Facility written sop during transportation to satellite site: N/A
Licenses to receive, store, dispense and return controlled substances
- Required Licenses or Registrations: No
- Does the Facility have the ability to handle radio-labelled Investigational Products? No
- Does the Facility have the ability to handle radio-labelled Investigational Products? No
Equipment
- Investigational Product:
- Centrifuge: Yes
- Refrigerated Centrifuge: No
- Centrifuge: Yes
- Refrigerated Centrifuge: No
Patient Records
- Record Archiving: Yes
- EMR/EHR systems: Other
- Has your Clinical Trial Site or Service been accredited? No
- Audit Type: Sponsor
- EMR/EHR systems: Other
- Has your Clinical Trial Site or Service been accredited? No
- Audit Type: Sponsor
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
Bacterial Infections and Mycoses
Cardiovascular
Digestive System Diseases
Endocrine System Diseases
Mental Health
Musculoskeletal Diseases
Nervous System Diseases
Nutritional and Metabolic Diseases
Occupational Diseases
Respiratory Tract Diseases
Skin and Connective Tissue Diseases
Virus Diseases
Wounds and Injuries
Study Types
Industry
Source Document Types
Paper and Electronic
Has your Clinical Trials Site or Service been audited by:
Sponsor
Average time to start study (in calendar days)
30-60
Support in-patient admissions
No
PK & PD specimens
Yes
Study Phase Capability
Phase II
Phase III
Phase IV
Type of Diagnostic Equipment
ECG/EKG Electrocardiogram
Patient Population
Healthy Volunteers
Adults 18 and onwards