Dossier compilation (CTD, ACTD, DMF, and another dossier as per National guideline)
Analytical method validation, Dissolution Profile
Expert Report-Quality, Clinical and Non-clinical
Prepare Summary of product (SmPC) and Pack Information Leaflet (PIL)
Prepare label and carton contents
Bioavailability / Bioequivalence / Clinical Trial Studies from DCGI approved lab
Nutraceuticals, Herbal products dossier and submission.
Reply to MOH queries
We provide contract manufacturing and prepare attractive artworks for samples.
Registration in ASEAN COUNTRIES (e.g. Myanmar, Cambodia, SriLanka, etc.), Francophone Countries (e.g. Mali, Liberia, Burkina Faso, etc.) , CIS Countries (e.g. Turkmenistan, Uzbekistan, Tajikistan etc.), LATAM – (Costa Rica, Peru/)
Our AIM
Long term Business relationship.