In international or multicenter clinical studies,laboratory dataoften originate from different laboratories that use varying measurement units (e.g., mg/dL vs. mmol/L). TheGood Clinical Data Management Practices (GCDMP, Chapter on CRF Design and Data Collection)provides clear guidance on managing this variability to ensuredata consistency,traceability, andminimized transcription errors.

The approach that results infewer transcription errorsis toallow sites to enter lab values exactly as recorded in the source document (original lab report)and to requireexplicit selection of the corresponding unitfrom a predefined list on the data collection form or within the electronic data capture (EDC) system. This method (Option B) preserves the original source data integrity while enabling centralized or automated unit conversion later during data cleaning or statistical processing.

Option B also supports compliance withICH E6 (R2) Good Clinical Practice (GCP), which mandates that transcribed data must remain consistent with the source documents. Attempting to derive units automatically (Option A) can lead to logical errors, while forcing sites to manually convert units (Option D) introduces unnecessary complexity and increases the risk of miscalculation or inconsistent conversions. Printing only standard units on the CRF (Option C) ignores local lab practices and can lead to discrepancies between CRF entries and source records, triggering numerous data queries.

TheGCDMPemphasizes that CRF design must account for local variations in measurement systems and ensure thatunit selection is structured (dropdowns, controlled lists)rather than free-text to prevent typographical errors and facilitate standardization during data transformation.

Therefore, OptionB—“Allow values to be entered as they are in the source and the selection of units on the data collection form”—is the most compliant, accurate, and efficient strategy for minimizing transcription errors in international lab data collection.

Reference (CCDM-Verified Sources):

Society for Clinical Data Management (SCDM), Good Clinical Data Management Practices (GCDMP), Chapter: CRF Design and Data Collection, Section 5.4 – Laboratory Data Management and Unit Handling

ICH E6 (R2) Good Clinical Practice, Section 5.18 – Data Handling and Record Retention

CDISC SDTM Implementation Guide, Section 6.3 – Handling of Laboratory Data and Standardized Units

FDA Guidance for Industry: Computerized Systems Used in Clinical Investigations, Section 6 – Source Data and Accuracy of Data Entry