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:

13

Years of experience in the Russian Federation

500+

Registered drugs

60+

Drugs on-going

45+

Submitted and accepted by the authorized federal body dossiers
in accordance with the EEU requirements 

CONTACTS

Russia, Moscow.

Multifanctional complex «Federation»
Presnenskaya embankment, 12
East Tower, 27th floor, 17 room.

© ARS PHARMRUSSIA: CLINICAL & REGULATORY EXPERT CRO, 2009-2024
All rights reserved.