SunGlow has an exclusive adept team with business edge to offer efficient and quality work with compliance to Global Regulatory standards. We focus on comprehensive services from Compilation of Dossier, Responding to recommendations and Approvals for Marketing authorizations.

We assist our customers with the following

  • Regulatory Due diligence
  • Pre-submission and / or scientific advice procedures
  • Dossier evaluation and Gap analyses in Technology Transfer projects
  • Writing chemical-pharmaceutical documentation (CMC, Module 3)
  • Writing and review of Clinical overviews (CO) and Non Clinical Overviews (NCO)
  • Writing quality overall summaries
  • Preparation , submission and management of all types of Marketing Authorization Applications

Sunglow Lifescience Private Limited

EU - GMP

TGA – Australia

Zimbabwe


Ethiopia

WHO GMP

Sunglow Pharmaceuticalss Private Limited

WHO GMP

FSSAI