ARS has significant experience in providing the following services:  

  Drugs registration

  Botanical drugs registration

  Dietary supplement registration

  Maximum sale price registration and re-registration

  Preparation and submission of documents required for GMP certificate obtainment

  Conducting independent inspections of drug manufacturing and/or preparation for the audit

  Bringing registration dossiers into conformity to the EEU requirements

  Making amendments to the document of registered drugs

  Confirmation of state registration (renewal of state registration)

  Technical dossier conversion into XML format (electronic dossier)

  Other consulting services on regulatory and intellectual issues in the pharmaceutical field

OUR COMPETITIVE ADVANTAGES: