CDMO
Small-molecule API CDMO services covering route scouting, process development, technology transfer, scale-up, and commercial GMP manufacturing. TBD Pharmatech supports niche-to-mid-volume API programs from development through EU-based GMP supply.
Analytical QC services
Analytical method development, validation, GMP release testing, stability studies, and quality-control support for small-molecule APIs, intermediates, and pharmaceutical materials. Available as part of integrated CDMO programs or as stand-alone analytical services.
QP and Quality Services
EU Qualified Person release, GMP batch certification, quality assurance, and CMC support for pharmaceutical materials and API supply chains. TBD Pharmatech supports compliant batch release and regulatory readiness from development through market supply.
RnD – custom synthesis Services
Laboratory-scale custom synthesis and small-scale development for complex small-molecule compounds, intermediates, reference materials, and conjugates.
CDMO – Contract manufacturing
Contract manufacturing for small-molecule APIs and intermediates, including process transfer, scale-up, and EU cGMP production. Supports clinical and commercial manufacturing with batch sizes from approximately 3–200 kg, including integrated analytical, quality, and regulatory support.
Sourcing & Distribution Services
Sourcing, storage, and distribution support for small molecule compounds. These services support secure pharmaceutical supply chains with qualified suppliers and quality assurance.
