CDMO
We offer integrated development and GMP manufacturing for small-molecule APIs and intermediates—from route design and pilot optimisation to multi-hundred-kilogram production. Your molecule stays in expert hands from first-in-human studies through commercial supply and full life-cycle management.
Analytical QC services
TBD Pharmatech offers comprehensive quality-control services such as method development, validation, GMP release testing and other. These capabilities are available both as part of an integrated development program but also as stand-alone analytical services.
QP and Quality Services
Guided by our QA specialists and Qualified Persons, TBD Pharmatech releases materials under EU GMP and verifies every batch against the highest regulatory standards. Flexible batch-release options and expert CMC support keep your project moving smoothly from development to market.
RnD – custom synthesis Services
TBD Pharmatech’s R&D team delivers custom synthesis of complex small-molecule compounds and conjugates at laboratory scale. Drawing on diverse multi-step and conjugation chemistries, supported by comprehensive in-house analytics, we rapidly supply precisely characterised materials that advance discovery, assay development, and pre-clinical studies.
