A) Pre & Post-Registration Activities of Pharmaceutical Products for All the Foreign Countries. (ROW countries)
New Registration/Renewal/Query of Pharmaceutical Products Workout/Activities –
B) Initial Feasibility of Product –> Legal Application –>Dossier (Technical Documents) Review/Finalization –> DMFs Review/Finalization -> Dossier Compilation –>
C) MOH/Client Conversation for Filling of Dossier –> Query Handling –> Commercialization of Product.
D) International Tender Work out
Technical Documents/Administrative Documents/Physical Sample Requirements/Legal Requirements/Form Submission and others – work out as per Guidelines of different Countries for timely submission.
