About Us

At Phareon Regulatory Solutions, we simplify global regulatory compliance for the pharmaceutical industry.
We specialize in dossier documentation, technical authoring, and regulatory submission support for drug products, APIs, and herbal formulations.

Our team brings together expertise in preparing CTD/eCTD, ACTD, and regional submissions, ensuring your products meet every national and international health authority requirement with precision and efficiency. From compiling complex scientific data to managing end-to-end submission lifecycles, Phareon stands as your trusted regulatory partner—helping you accelerate approvals and maintain compliance seamlessly.

We combine deep domain knowledge, global regulatory insight, and quality-driven processes to deliver documentation that reflects accuracy, consistency, and compliance at every stage of product development.