Your
passageway
between the
Middle East
Iran and
Europe
Representation in the Middle East, Iran and Europe
Regulatory expertise
Evolving towards an eCTD
Optimise eCTD lifecycle management
Organising special events, workshops and trainings
Situated at the heart of Europe,
in the vicinity of Brussels, capital of Belgium
and home base of the European Commission.
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Representation of your company in the Middle East and Iran / Europe
ATREXFI represents your company at the Pharma and BioTech events in the Middle East and Iran.
Training and knowledge transfer
Workshops on eCTD, CTD and NeeS
Workshops on Life Cycle Management
Exchange of ideas between the different regions on registration guidelines.
eCTD Consultancy for your submission in Europe
The regulatory approval for a eCTD (electronic common technical document) is of vital importance to the client as this is the point from which the commercialization of a drug can start.
ATREXFI , in close cooperation with the client, sets up an overall project plan, defining the different steps in the process towards a regulatory compliant dossier for Europe.
This implies a maturity test of your company and following the results of this maturity test a design of growth path to eCTD maturity.
ATREXFI works closely together with specialised companies that can perform the eCTD for your company from the beginning up to the send off to the European authorities.
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