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Complion is a 21 CFR Part 11 compliant electronic document storage platform that may be used for regulatory and research participant records generated for clinical trials. The application supports remote monitoring, eSignature, and centralized document management to facilitate digital documentation compliance, address physical document storage constraints, and promote information sharing with sponsors and CROs.

To get started in Complion, a member of the study team must submit a request to have a new study built in Complion via SIFTER. The request for a new study build should identify study team members who will need access. If a study team member does not already have an active Complion user account, one will be created.

How To Activate Your Account

  • You will receive an email notification from Complion prompting you to click the link provided
  • Use your CHOP email and network password to login for the first time
  • Upon logging in, you will be prompted to complete required Complion eLearning
  • After attesting to the completion of eLearning, new user account activation in Complion is complete

Study teams are not required to use Complion. However, adoption is encouraged. The platform ensures the highest level of compliance without the tediousness of paperwork, allowing investigators to spend more time with their trials. Remote access to regulatory documentation also supports expedited startup and increased communication among study team members and sponsors.