We support pharmaceutical and biotech manufacturers with fine chemical synthesis, cGMP documentation, and resilient supply programs built around audited process knowledge.
Learn about the program
Lonza aligns synthesis, analytics, scale-up, and regulatory evidence so development teams can progress without separating science from manufacturability.
Route scouts evaluate yield, impurity fate, solvent class, and isolation behavior before transfer decisions are locked.
Kg-to-ton campaigns use controlled change records, analytical comparability, and clear batch genealogy for regulated buyers.
Documentation can include CoA, SDS, residual solvent logic, HPLC purity method, and supplier qualification support.
Support clinical and commercial supply chains with impurity control, solvent strategy, and documented process transfer.
Explore Pharmaceutical solutions
Match supply documentation, change control cadence, and release testing to biologics manufacturing expectations.
Explore Biotechnology solutions
Coordinate reaction hazard reviews, containment requirements, and analytical release standards before scale-up.
Explore Specialty Chemistry solutionsLonza's sustainability program connects climate, water, responsible operations, and patient-centered supply. Progress claims are tied to defined methodologies, including Scope 1 and 2 emissions accounting, water withdrawal tracking, and externally reviewed ESG disclosures.
Training and EHSS routines keep production decisions tied to operator protection and accountable review.
Learn moreEnergy, waste, and water projects are reported with baselines, boundaries, and measured progress.
Learn moreProcess intensification teams examine solvent recovery, yield improvement, and contained handling.
Learn moreCommercial programs define service levels, audit cadence, and change notification expectations.
Learn moreHow document control reduces avoidable release questions.
Method alignment before scale-up reduces revalidation loops.
Traceable records help procurement teams manage risk.
Solvent class, impurity purge, and isolation profile all matter.
Documentation clarity starts before a campaign is booked.
Scale-up decisions rely on thermal and analytical evidence.
A practical session for strategic sourcing and quality leaders.
Meet technical specialists for dossier and audit planning.
Discuss recovery, substitution, and lifecycle documentation.
New chromatography workflows improve impurity monitoring.
Supplier review expands to high-impact raw materials.
Scheduled updates improve SDS and CoA search performance.