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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.
Serbia
Legislations
  1. Law for Drugs and Pharmacies of the Republic of Serbia No. 84/2004

Regulations (MOH):
  1. Regulation on Conducting Drug Clinical Trials on Human Subjects
  2. Regulation for Conducting Clinical Trials
  		 


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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