• Full-service capabilities resulting in cost- and process-effectiveness
  • CRO staff:
    • almost all CRAs are MDs or have degree in science (very often are former co-investigators)
    • site training
    • clinical supply activities & issues resolution
    • much more time spent with investigators
    • very high motivation

Our local CRA can communicate and conduct activities by minimizing local cultural and administrative hurdles. In additona Comac Medical can easily reallocate  additional support of CRAs, project leaders, regulatory advisers and many other clinical research specialists, as our business model is flexible and adaptive to the clients needs.

  • Access to large (drug naive) patient pools
  • Qualified staff, highly experienced in wide range of therapeutic areas; trained in ICH-GCP, relevant regulations, standards and company SOPs
  • Flexible service offers to meet the needs of the client and project
  • Upfront strategic planning to ensure a clear development plan
  • Collaborative partnership with clients based on open communications
  • Rapid study start-up and fast enrollment
  • Protocol and documentation design and preparation
  • Dedicated clinical and monitoring teams
  • In-House Data Management, Biostatistics, Medical Writing and QA