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• Ravinder Singh
  FDA Releases Updated RTA Checklist
  
  The guidance replaces the 30 October 2017 draft guidance of the same name and describes the administrative steps #FDA will take to either Refuse to Accept (RTA) or file a request for an evaluation of automatic class...  moreFDA Releases Updated RTA Checklist
  
  The guidance replaces the 30 October 2017 draft guidance of the same name and describes the administrative steps #FDA will take to either Refuse to Accept (RTA) or file a request for an evaluation of automatic class III designation (De Novo request).
  
  https://lnkd.in/fx2ABH6
  
  Read More: https://bit.ly/2pe7Qws  less

  October 10, 2019

  

  FDA Releases Updated RTA Checklist
  
  The guidance replaces the 30 October 2017 draft guidance of the same name and describes the administrative steps #FDA will take to either Refuse to Accept (RTA) or file a request for an evaluation of automatic class...  moreFDA Releases Updated RTA Checklist
  
  The guidance replaces the 30 October 2017 draft guidance of the same name and describes the administrative steps #FDA will take to either Refuse to Accept (RTA) or file a request for an evaluation of automatic class III designation (De Novo request).
  
  https://lnkd.in/fx2ABH6
  
  Read More: https://bit.ly/2pe7Qws  

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• Ravinder Singh
  The #FDA has released draft guidance for using the Inactive Ingredients #Database to aid drug developers.
  
  The US Food and Drug Administration (FDA) has released draft guidance for public consultation on the use of the Inactive Ingredient Database...  moreThe #FDA has released draft guidance for using the Inactive Ingredients #Database to aid drug developers.
  
  The US Food and Drug Administration (FDA) has released draft guidance for public consultation on the use of the Inactive Ingredient Database (IID).
  
  Read More: https://lnkd.in/fieVJYv  

  July 19, 2019

  

  The #FDA has released draft guidance for using the Inactive Ingredients #Database to aid drug developers.
  
  The US Food and Drug Administration (FDA) has released draft guidance for public consultation on the use of the Inactive Ingredient Database...  moreThe #FDA has released draft guidance for using the Inactive Ingredients #Database to aid drug developers.
  
  The US Food and Drug Administration (FDA) has released draft guidance for public consultation on the use of the Inactive Ingredient Database (IID).
  
  Read More: https://lnkd.in/fieVJYv