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Services

 

Clinical Project Management

Clinical Operations

Clinical Data Management

Biostatistics

Medical Writing

Clinical Quality Assurance

Clinical Resourcing

Functional Service Teams

Technology


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Clinical Data Management - CRF Tracking

Peachtree will receive, log and track CRFs. Our tracking process will include the following:

  • Tracking and documenting the flow of the CRFs send from sites to Peachtee.
  • Reconciliation of CRF Data entered against CRFs received
  • Procedures for confirmation of the receipt/non-receipt of CRFs

CRFs will be held in a secure, fireproof environment until scanning and data entry is complete; after which, we will return these CRFs to the sponsor on an ongoing basis.

Scanning and Data Entry

Peachtree will perform scanning of original CRF and DCF documents.  At the end of the study, the sponsor receive one PDF file per subject, containing all CRFs and DCFs for that subject.

Peachtree will write study specific data entry conventions which will be finalized prior to data entry beginning.  We will perform interactive double data entry.  Textual data will be entered once and sight verified by a second data entry operator.  Investigator verbatim terms (i.e. terms to be coded) will be double data entered. 

 

 
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