Your clinical trials will be conducted in an accurate and seamless manner through implementation of our highly efficient and professional monitoring activities.

Service Features

Point 1.
Project management by capable project leaders well-versed in GCP.
Point 2.
High-quality service by our integral team including data management and biostatistics to fulfill your application targets.
Point 3.
RBM approach (placement of persons with experience in RBM studies, appropriate building in quality (BiQ), risk detection/prevention effects by selected KRIs)

Main Services with Details

  • Consultation throughout the entire clinical development
  • Management of overall clinical trial projects
  • Clinical trial coordinating secretariat duties
  • Support for preparation of protocol (draft)
  • Support for preparation of subject informed consent form (draft)
  • Support for preparation of investigator’s brochure (draft)
  • Feasibility studies
  • Selection of clinical trial sites
  • Handling of contracts and requests for clinical trials
  • Collection and shipment of investigational drugs
  • Management of cases and progress of the project
  • Direct access and SDV
  • CRF collection and data cleaning
  • Termination proceedings for clinical trials
  • Process-focused QC activities

ADDIN SMALLT(EDC system for post-marketing surveillance)

Our EDC System with speed, low cost and high-quality has been released

For more details

For further information onINTAGE Healthcare Inc.

If you have any questions or comments, please do not hesitate to contact us.

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INTAGE Healthcare’s Scope of Service