Trial Planner

Throughout the process of designing, setting up and running a clinical trial, CNS provides a quality service with its experience in planning, monitoring, reviewing and reporting of clinical trials.

Our Trial Planner service represents an expansion on traditional CRO services where CNS works collaboratively with our clients to firstly ensure Australia is the best place for their initial trials and through that feasibility work closely with the client and our network of phase I units, SMOs and therapeutic specialists/clinicians to ensure the best possible solution is developed to meet our clients' goals such as market driven timelines, investor needs and regulatory expectations.  

Typical areas where CNS assists our clients in trial planning are:

• Site/recruitment feasibility
• Protocol design and development
• Investigator Brochure (IB) writing
• CRF design & printing
• Independent Toxicological Review/Reporting
• Australasian trial sponsorship where international clients do not have a local subsidiary or partner
• Advice on importation/customs and assistance with shipping strategies
• Clinical Trial Insurance

Furthermore, CNS can also support these services in the USA, Europe and New Zealand through our strategic partners as well as additional support including:

• Funding and Investment Consultancy
• Australasian, US & European Union regulatory consultancy - small molecules, biologicals and devices
• Pre-clinical and ADME services
• Analytical Analysis - development, tech transfer and existing validated assays
• Initial Market Analysis and Product Positioning
• GMP Manufacturing
• Secondary packaging, storage & distribution