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14 August 2013
On July 8 2013 the Food and Drug Administration (FDA) announced the availability of draft guidance, Medical Device Reporting for Manufacturers, which, when final, will supersede the 1997 version. The draft addresses specific questions about the reporting and record-keeping requirements for device-related adverse events.
The draft significantly expands on the earlier guidance for manufacturers and attempts to respond to the practical concerns of industry. For example, it includes recommendations concerning:
One of the most difficult issues that manufacturers face is determining whether an event is reportable. The draft contains some suggestions on this topic, including events involving:
The draft makes additional practical recommendations concerning the information that should be submitted in the different blocks on the MedWatch Form 3500A. Finally, the draft makes clear that certain changes to medical device reporting proposed by Congress in the Food and Drug Administration Amendments Act 2007 have not been implemented by the FDA. The result is that malfunction reporting requirements for Class I and those Class II devices that are not permanently implantable, life supporting or life sustaining, continue to be subject to the medical device reporting requirements of 21 CFR Part 803.
The draft guidance is available online(1) and comments should be submitted by October 7 2013.
For further information on this topic please contact Raymond A Bonner or Coleen Klasmeier at Sidley Austin LLP by telephone (+1 202 736 8600), fax (+1 202 736 8711) or email (email@example.com or firstname.lastname@example.org).
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Raymond A Bonner