You decide at what level you want to involve our services in your project and at what stage you want to delegate specific tasks: it’s up to you!


  1. You can use the platform to independently manage prototyping, eCRF configuration, Data Management.
  2. You can consider us an extension of your data management team and share an activity & responsibility plan.
    Because the more you rely on ACTide prototyping tools and workflow, the more efficient and properly documented methodology is shared by the two teams.
  3. You can entrust us with the full service, up to biostatistics.


Main Services

  • Clinical Data Management (ACTide Power DM)
  • Medical Coding (MedDRA, WHO Drug / ATC / ICD dictionaries)
  • Study Level Validation
  • Data Integration and Feed
  • Study Migrations
  • SDTM DB Migration
  • Implementation of SDTM, ADaM and define.xml for FDA/PMDA submission
  • CDISC/CDASH compliant eCRF
  • Biostatistics
  • Unblinding envelopes delivery
  • Online Training; Teach Yourself Training programs for Clinical Sites


Time & Budget

  • Your success depends on meeting or exceeding deadlines
  • Forms configuration instead of custom software development



Your study deserves nothing short than unequivocal compliance

Time & Budget

High productivity performance
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Products & Services

ACTide Clinical Data Service for your clinical trial 
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Latest news

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Merry Christmas and Happy new Year

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