Your Preferred Global Clinical Research Organization
Research and development sponsors are challenged to dramatically improve efficiencies, reduce costs and speed cycle times – all while maintaining the highest standards of quality in their clinical development projects and programs.
Clinlogix meets this imperative, focusing on excellence in innovation and consistently surpassing the expectations of clients in the pharmaceutical, biotech and medical device industries. It is our expert ability to consult with our clients to understand and assist in defining those needs. Our ability to execute and deliver these services is unparalleled. We offer the depth and breadth of expertise and resources necessary to assist managing full clinical trials, as well as the flexibility to serve a client’s particular needs.
Our innovative virtual clinical development pathway, offers our clients access to the infrastructure and expertise necessary to support their clinical development. Similar to a Functional Service Provider (FSP) model, our process allows us to unbundle core and non-core functional areas of clinical research while maximizing efficiencies, cost savings and maintaining our high level of quality. This approach gives Clinlogix clients the ability and access to choose the level of service and participation as they require for their specific project. Full-service clinical development or functional services as needed, globally or regionally, from Discovery through Phase I-IV clinical trials – and anywhere in between.
Our Team structure is designed to provide direct communication and accountability between team members and our clients. We ensure that the entire process is open and transparent for all stakeholders – our clients, our investigators, the investigative sites, and our study participants. Our teams are designed to facilitate the sharing of responsibility and ownership on every project, empowering everyone to constantly identify, assess, and manage risk.
Choose the Expertise You Need
Full-scale and FSP services are offered in more than a dozen therapeutic specialties include:
- Site Identification
- Study start-up
- Contract and Budget Management
- Data Management
- Project Management
- Regulatory services
- Safety Management
Contact us today for a consultation about the services we can provide to bring your next clinical trial or program to an on-time, on-budget, compliant and quality conclusion.