Development stage: Phase I

For Phase I clinical trials, we offer a single point of contact for all clinical supply management matters from API bulk reception through drug formulation, patient administration and bio-analyses. We can offer full support or assist you in the individual services you need, such as:

Stability testing

Stability testing is performed after storage in defined conditions according to standard and accelerated ICH conditions. We provide you with different range of storage conditions. All storage rooms are fully-controlled with 24/7 monitoring and alert systems. Our services include: Support in designing studies for real-time Development and validation of “stability indicating methods” Examination of stability-relevant […]

Drug administration & Patient monitoring

Centralized clinical unit with 30 equipped hospital beds Experience in running different study types and trial design Different types of drugs like NCE and NBE Database of more than 2.700 healthy and reliable volunteers Privileged access to medical and technical expertise of CHU and ULg (such as Cyclotron, GIGA, CIP, Sleep Center, Pain clinic…) We offer […]

Bio-analysis

Standard biology analysis: certification for more than 550 tests, 17025 and 15189 ISO standards and BELAC accreditation Development of personalized drug monitoring Determination of IMP, metabolites and drug residues in different biological matrices PK, PD and immunogenicity testing Looking for clinical advice or support, or preparing for a clinical study? We will help you set up […]