Arion Group is deeply committed to quality manufacturing and patient safety, using a Pharmacovigilance system for efficient identification and communication of medicine-related adverse events.
Qualified & enrich experience RA team with eCTD, ACTD & Country Specific dossiers submission. Having 165 dossiers / CoPP with Arion Group for exports. Our DRA is completely integrated regulatory solution for our buyers that complies electronic submission of
Dossiers in eCTD format including DMF Submissions.
Quick and intuitive construction of complex electronic submission for any regulatory
authority .
Multi-country submissions with country specific requirements as per the compliant.
Mapping of documents within regional submissions.
Up-to-date eCTD versions inclusive of accurate eCTD Modules, eCTD format, eCTD
Structure.
Dossier assembly and compilation in eCTD format
initiated the implementation of electronic application (eCTD).
The name, Arion Group is regarded as a hallmark of excellent quality standards across the globe. We maintain a strong culture of quality consciousness, which is incorporated across our every operation. Thus, each of our manufacturing facilities are regularly inspected and audited as per cGMP guidelines which are laid down by leading regulatory authorities and our products are under registration in many International authorities such as the DAV Vietnam , FDA Philippines, Myanmar , MoH Cambodia, MoPH Afghanistan, MoPHP Yemen, MoH Iraq FDA Ghana, AIRP Ivory Coast, ABRP Benin, DPML Cameroon, Burkina Faso, Togo, DEGIMED Peru, Guatemala, MoH Bolivia, Venezuela, Ecuador, Honduras, Tajikistan & Other Africa, Asian, CIS Countries.
Bhutan
Malaysia
Chile
Oman
Iran
Jordan
Morocco
Nigeria
Botswana
Ethiopia
Uganda
Zambia
Tanzania
Bhutan
Malaysia
Chile
Oman