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Custom synthesis, building blocks and small‑molecule services from discovery to GMP, backed by analytics, QA and resilient finishing & logistics.
From early clinical to commercial supply with tech transfer.
Regulatory-ready reagents, buffers, excipients and adjuvants.
Bioconjugation and complex chemistries with controlled environments.
Route scouting to kilo scale for complex small molecules and linkers.
Key intermediates, reference standards and specialty reagents.
Process engineering, validation strategy and GMP pathways.
Fit‑for‑purpose methods, LC‑MS/NMR, stability and impurity profiling.
PQS aligned with ICH; data integrity (ALCOA+) and change control.
Sourcing, warehousing, repackaging and temperature‑controlled shipping.
Qualified supply chain with dual‑sourcing and vendor audits.
From gram vials to drums with labeling and COAs.
Temperature‑controlled storage and inventory traceability.
Cold‑chain and DG shipping with documentation.
Ensuring all operations strictly follow GMP, ISO, and regulatory standards to maintain consistent quality, traceability, and customer confidence.
Expertise in designing and synthesizing complex heterocyclic and chiral building blocks.
Skilled handling of air- and moisture-sensitive reactions under controlled cryogenic conditions.
Custom linker and conjugation strategies integrating peptides with small molecules.
Efficient catalyst evaluation and process optimization using Design of Experiments (DoE).
