CDMO

TBD Pharmatech provides small-molecule API CDMO services, including route scouting, process development, technology transfer, scale-up, and GMP manufacturing for pharmaceutical and biotech companies. We support projects from early development through commercial production, with EU cGMP manufacturing in Estonia and a focus on niche-to-mid-volume APIs (3–200 kg).

We provide

• Route scouting and synthetic route design

• Regulatory support (ASMF, DMF, CMC)

• Process development and optimization

• Analytical method development and validation

• Scale-up from laboratory to production

• Technology transfer to GMP manufacturing

When to work with TBD Pharmatech

• When you need small-molecule API process development

• When you need to scale up from lab to GMP manufacturing

• When you require EU-based small molecule production

• When your project involves niche or mid-volume GMP compounds

• When you need technology transfer into manufacturing

Manufacturing scale

• Development and pilot scale

• Mid-scale production: 3-20 kg per batch

• Larger scale production: up to 200 kg per batch