As we are handling international business in addition to our national operations, we have a dedicated and efficient regulatory team. We are working in different regions of the world and catering dossier requirements in line with CTD, ACTD and NeeS.
We are working in both pharmaceutical and medical device category depending on the need of different countries. Our regulatory analysis also includes GMP analysis and we work on the international standards. We have already received GMP of Sudan, Ivory Coast and Sri Lanka. We have followed ICH, WHO and FDA guidelines in order to meet the international standards.