Accelerating your clinical development program from Project Management through to clinical trial monitoring, management and patient recruitment.
Telstra’s streamlined and integrated clinical trial services are delivered by a dedicated team of professionals with deep industry and therapeutic area expertise across all phases of clinical development.
This, coupled with our deep understanding of operations in the American countries and strong relationships with trial sites - results in an efficient and effective trial start-up and recruitment of patients to achieve your goals.
Telstra Research is a fully Quality Endorsed Company compliant to the ISO9001:2000 standard, which means a structured, professional approach to all phases of your clinical research trial, from administrative requirements, contract and operational issues through to reporting and communication needs.
Telstra’s registration clinical trials services are designed specifically for sponsors without local presence in the countries in which we operate. In particular the depth of our regulatory expertise across the region adds clarity and transparency to the trial startup process.
Our customized service means all facets of a trial are covered by the one contract, including third party vendor management and local site agreements, making working with us a simple and streamlined process.
Feasibility assessment and site selection
Protocol development & CRF design
Patient recruitment strategies
Ethics Committee and Regulatory submissions
Project management and monitoring for Phase I-IV trials
Full biometrics services, including randomization and IWRS services
Local sponsorship
Third party vendor management
Medical, technical and CSR writing
Drug depot and logistics providers
Central laboratories
Translation service providers where required
Phase I units
Event managers (Investigators’ Meetings)
Telecommunication brokers (indemnities)