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med tech software solution

  • sakshamapp
  • Jun 20, 2017
  • 1 min read

The MedTech conference once again opened the debate on how to structure regulations. Now that the focus has shifted towards value based healthcare, the need to have rules that support that approach becomes more evident. Companies are increasingly adhering to the MedTech code and shifting away from direct sponsorship to better educate the business and involve more stakeholders. But how can we better talk to regulators so that we may come to a more widely accepted and workable code? There is a need for cross-functional collaboration with Subject Matter Experts in the Medical Device field, where knowledge is shared among legislators, lawyers, compliance officers, purchasers, etc. On a global scale, governments are far from aligned on codes and regulation, as this is a long and tedious process. med tech software solution


 
 
 

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