IT Services

MoPS, LIMS and SEND: software that keeps sponsors informed and study data submission-ready.

MoPS

Management of Project Schedule

Stay on top of your project with MoPS

Our real-time project schedule management program, MoPS, enables seamless communication with sponsors, allowing them to track phased progress in real time via web e-mail. Collaborate efficiently and share progress internally with ease.

MoPS screens: a sponsor's study dashboard and the detailed progress timeline of a 4-week repeated-dose study in rats (Korean interface)
LIMS

Laboratory Information Management System

Enhance study reliability with our Laboratory Information Management System (LIMS). LIMS automatically connects to SEND (Standard for Exchange of Nonclinical Data) for U.S. FDA IND or NDA approval, ensuring accurate data exchange for regulatory compliance.

LIMS programs

  • General toxicity
  • Reproductive toxicity
  • Immunotoxicity
  • Local toxicity
  • Genotoxicity
  • Safety pharmacology
  • Ecotoxicology
  • Clinical pathology
  • Tissue pathology
SEND

Standard for Exchange of Nonclinical Data

Meet FDA requirements with SEND, the Standard for Exchange of Nonclinical Data. We provide not only our own study data but also legacy study data from other test facilities using our own SEND software program. Submit study data in SEND format, including Final Report, SEND dataset, Define File and nSDRG, with confidence.

  1. In

    Data sources

    • LIMS: clinical signs, body weight, pathology, bioanalysis
    • Raw data from the sponsor
    • Raw data from other facilities
  2. →

    SEND solution (including conversion)

  3. Out

    Submission

    CDISC · FDA · PHUSE

Contact Dt&CRO for reliable IT services that streamline your preclinical trial data management. Gain regulatory compliance and efficiency for successful drug development.