SunGlow has an experienced team with business edge to offer efficient and quality work with compliance to global regulatory standards. We focus on comprehensive compilation of dossier(s), responding to recommendations and approvals for Marketing Authorizations.

Key Roles in Regulatory

  • Preparation, submission and management of all types of Marketing Authorization Applications.
  • Dossier evaluation and Gap analyses in Technology Transfer projects
  • Writing Quality Overall Summaries
  • Writing Chemical and Pharmaceutical documentation (CMC, Module 3)

Sunglow Lifescience Private Limited

WHO GMP

TGA – Australia

Sunglow Pharmaceuticalss Private Limited

WHO GMP

FSSAI