Dokumeds has partnered with Clarivate to provide Regulatory Expertise in a further module of their Cortellis Regulatory Database.


Dokumeds has worked with Clarivate Analytics since 2003, and is responsible for maintenance services of Drug module Regulatory summaries for the Baltics, monitoring  

  • any publication of new legislation, regulation and/or implementation rules;  
  • administrative or scientific guidelines and forms related to pharmaceutical products and any amendment to the same;  
  • any possibility of change (amendment, draft legislation and/or regulation) or forthcoming changes related to the scope of Cortellis Regulatory Intelligence business.  

In 2018 Dokumeds will develop regulatory summaries explaining the Baltic’s regulatory environment for medical devices, in vitro diagnostics and combination products, further extending Dokumeds inhouse regulatory expertise.

 


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