Our Process

A structured, end-to-end approach ensuring speed, quality, and regulatory excellence from concept to commercial success.

01
Scope & Strategy

TPP definition, regulatory pathway, and comprehensive risk mapping.

02
Design & Plan

Protocol & CMC planning, budgeting, and quality strategy alignment.

03
Execute

Clinical execution and manufacturing with integrated QA oversight.

04
Release & Submit

Database lock, submission packages, and QA-approved product release.

05
Scale & Sustain

PPQ execution, commercial manufacturing, and lifecycle management.

Indicative Timelines

FIH Start Up
8–12 Weeks
Phase 2 Start Up
12–16 Weeks
Tech Transfer to GMP
10–14 Weeks
PPQ to Commercial
12–20 Weeks