Regulatory Support

We are contributing to the ever-growing pharmaceutical industry, and we are doing it through government regulations and policy. We believe in a lawful and good practice and are making sure we always follow all regulations. We provide comprehensive regulatory support for registration and marketing to our clients with their products. This includes assistance with document preparation, regulatory strategy development, and navigating the approval process. 

We have teams of experts who will guide you through the process and provide all sorts of support till the approvals. These are the required documents for registration of pharmaceutical products that we provide help with:

  • CTD and ACTD Dossiers for all products.
  • Certificate of analysis (COA).
  • free sale Certificate (FSC) certificate
  • Bioequivalence (BE) study for selected products. 

Through our established network and production system, we are able to provide the best products at the best price point. That gives us an edge in thriving in the world and entering different markets. Currently, we are supplying healthcare products in Asia, Europe, Africa, South America, and the Middle East.