Almac Sciences
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CDMO
Business Category : Drug Substance, Drug Additives, Intermediate、CMO、Contract Service- Analysis & test 、Pharmaceutical manufacturing、Chemical product manufacturing
Main Service Region : Japan、United States、Korea, Republic of、Taiwan、Europe(excluding UK)、United Kingdom
Product & Service
Analytical Services
Service Category :Analysis
From our state-of-the-art FDA and MHRA audited laboratories in the UK, Europe and US, we employ over 150 highly trained analytical scientists with expertise in all areas of drug development, including small molecules, peptides, conjugates and potent materials. Our European laboratory is Ireland’s leading GMP, GLP (INAB) and GCP analytical support provider and fully certified contract laboratory.
Drawing upon our vast pool of scientific knowledge, we can greatly reduce the analytical challenges that typically arise during drug development.
Utilising a wide range of instrumentation, Almac will deliver fit-for-purpose solutions to match your analytical requirements.
Clients who use Almac to release drug substance and drug product in the EU and US benefit from shortened transfer time, cost savings and minimized disruption thanks to scientific and procedural continuity. Almac is unmatched in its ability to manufacture clinical trial supplies and provide analytical support.
“Almac’s Analytical Team continually demonstrate that we can rely on their services and timelines as promised.”
Client Testimonial
Why choose Almac for analytical services?
Communication and scientific continuity and key, whether your analytical requirements are stand-alone or form part of a drug development or commercial manufacture project. Our analytical scientists work with our drug substance and drug product formulation scientists, forming an integral part of the project team. This means they can share data, easily coordinate planning and scheduling, and deliver maximum efficiency.