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Q of the week

Q: Do clinical trials ever go wrong?

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Prototype devices

It is recognized that a manufacturer may wish to submit a small number  of "prototype models" of a device to clinical investigation in order to assess safety and/or performance; and those such prototypes may need to undergo a number of changes prior to large-scale production.



  1. Personal Data Protection Act No. 25.326 (2000)
  1. MOH: Ministerial Resolution1490/2007 Approving the Good Clinical Practice Guideline for Clinical Research with Human Beings    
  2. ANMAT: Provision 5330/97 on General Guidelines for the Conduct of Clinical Trials (1997) (Spanish)




Opinion Poll

Which one of the following do you think is the most common reason for participating in clinical trials?
This opinion poll provides an informal way for the clinical research community to express its views on current topics. The results are not a scientific poll and do not necessarily reflect the percentages of all clinical researchers who agree with these positions.
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