CDMO

TBD Pharmatech delivers small-molecule CDMO services built around three pillars—development, tech transfer, and commercial GMP manufacturing. Choose a fully integrated pathway or select only the modules you need; we can just as readily import an established process into our suites as we can design one from scratch.

1. Tech transfer

• Structured data review, gap analysis, and risk assessment

• Engineering runs and demonstration batches under our quality system

2. Development toolbox

• Route scouting and synthetic design

• Process optimisation and robustness studies

• Scale-up to kilo-lab and multi-hundred-kilogram batches

• Analytical method development and validation

• GMP documentation, stability studies, and regulatory dossiers (ASMF / DMF / CMC)

3. Commercial manufacturing

• Process validation, in-line quality control, and Qualified Person release

• Secure EU supply of validated API at the scale your market requires

This three-part framework gives you cost-effective, reliable, and flexible support strengthening supply security and moving your molecule to market with confidence.