ARS has significant experience in providing the following services:
Botanical medicines 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:
Years of experience in the Russian Federation
Submitted and accepted by the authorized federal body dossiers in accordance with the EEU requirementsгласно требованиям ЕАЭС
Multifanctional complex «Federation»
Presnenskaya embankment, 12
East Tower, 27th floor, 17 room.
PHONE + 7 495 374-62-84
contact us by email,
or fill out the request form.
© ARS PHARMRUSSIA: CLINICAL & REGULATORY EXPERT CRO, 2009-2020
All rights reserved.