CRO Services Overview
Cmed has grown every year since we began providing Data Management services in 2001. Customers regularly return for repeat business, with new customers approaching us following positive word of mouth recommendation from industry colleagues, affirming that we are becoming a leading global force in the industry.
Our clinical operations activities, such as Clinical Project Management and monitoring, are now also receiving immense praise. With additional specialist expertise in conducting Phase I studies, adaptive trials, oncology, anaesthesia and diabetes programmes, Cmed can be trusted with your most important projects.
Cmed has delivered many pivotal health authority audited trials, including full Phase III programmes, for some of the world’s best known companies.
Our services are characterised by:
- Investigator-centric focus
- Flexible solutions to meet your needs
- Specialists in clinical operations aligned with smart data acquisition and management
- Cost-effective solutions
- A reliable, quality, friendly service
The CRO Services:
- Clinical Project Management
- Monitoring
- Data Management (eDC & paper CRFs)
- Biostatistics
- Medical Writing
EDC technology services:
- Global license
- Trial licenses
- Hosting
- Help desk & support
- Online training services
With a full array of services, our clients can choose just one vendor to handle all their EDC needs, CRO needs and any combination of services. By providing the option of a customised solution, our clients receive the services best suited to them, rather than the vendor. The advantages of dealing with just one vendor include:
- Flexibility to evolve or change the solution(s)
- Attractive, low risk entry model for pharma of any size to “try before you buy”
- Long-term partner approach
- Future orientated solution(s)
