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Compliance In Focus
Posted by Sandra Maddock on Wed, Jan 23, 2013

Is Device Monitoring More Than SDV?

Source Data VerificationMany believe good monitoring should heavily focus on Source Data Verification (SDV), which stripped down to its simplest meaning equates to “X=X” and “Y=Y”.  And maybe some of you reading this are thinking “Isn’t that exactly what monitoring is?”  While data integrity is absolutely essential, it is only the beginning of what comprehensive monitoring encompasses.

The key to describing the critical role of a device monitor lies with 21 CFR  812.46, which states: 

  • Sponsor should secure compliance through monitoring of investigations
  • If an investigator is not complying with the investigator agreement, protocol, federal regulations, IRB requirements...device shipments should be discontinued and the investigators participation should be terminated

Therefore, to adequately fulfill regulatory requirements, monitors need to have solid knowledge of the agreement, protocol, regulations and IRB requirements in order to recognize non-compliance.  SDV only goes so far, leaving a huge gap in expectations and practice.

Monitors out in the field are bogged down with pressures to get through certain amounts of data, assist with query resolution, and other tasks associated with SDV.  As a result, the highest number of warning letter citations issued were not related to data at all, but to compliance with the protocol and investigator agreement.

Has anyone else experienced situations where this misalignment between project expectations and regulatory expectations have led to less than favorable results?

Photo Credit: Tilemahos Efthimiadis

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Topics: Medical Devices, Source Data Verification, Clinical Monitoring

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