About SGS Clinical Research
With over 40 years of experience as a mid-sized full-service contract research organization (CRO), we are a trusted partner in early-phase drug development. With our good manufacturing practices (GMP) production facility integrated into our clinical pharmacology unit in Belgium, we combine global standards with local regulatory intelligence and operational agility.
Our campus in Antwerp, Belgium, brings together a unique constellation of services – clinical pharmacology, laboratory services and GMP production – all in one state-of-the-art facility. This setup allows us to stay agile, compress timelines, reduce coordination overhead and respond quickly to your study needs. In combination with our contract development and manufacturing organization (CDMO) in the UK, we provide a seamless continuum of services:
from formulation development through to import, qualified person (QP) release, clinical packaging, dispensing and on-site administration. Already working with a CDMO? No problem. We pick up where they leave off, managing EU QP release of investigational medicinal product (IMP), production, packaging, labeling, dispensing and administration – all in one smooth, integrated process.
When you need to be sure, choose SGS.
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