Services

CDMO

TBD Pharmatech delivers small-molecule CDMO services built around three pillars — Development, Tech Transfer, and Commercial GMP Manufacturing.

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.

GDP Sourcing & Distribution Services

TBD Pharmatech’s GDP-licensed supply-chain team secures qualified raw materials and intermediates, manages temperature-controlled storage, and ships finished goods under full traceability. Our end-to-end oversight safeguards timelines and regulatory compliance while reinforcing the reliability of our partner's supply chain.