Clinical imaging

Together, the CHU and the GIGA have a vast expertise in clinical imaging techniques, individually or combined in a multimodal functional imaging approach.

Motion analysis

We can offer you a fully integrated analysis of the subject including spatio-temporal parameters (step frequency, step length, velocity, single and double support time…) and kinematics parameters (angular range of motion, velocity, ground reaction forces, muscles activity). Tests are performed in a 27 meters long-room (ensuring that subjects reach stabilized gait) in which the equipment can be used simultaneously and be synchronized on demand.

 

Safety (Phase I)

Patient administration:

  • 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…)

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We offer you a professional and scientific support to conduct clinical trials and the decision making processes during the early phases of the development of new molecules. This includes clinical pharmacology trials giving an insight into a drug candidate’s safety, tolerability, pharmacokinetics and pharmacodynamics.

Contact [info@b2h.be] us to discuss how these capabilities can forward your projects! We will help you develop tailored solutions.


Efficacy/tolerability clinical trials (Phase IIa to III)

The CHU de Liège has in-depth expertise in various therapeutic fields.

Thanks to our unique regional location, we have a quick access to a large and available network of all kinds of patients.

We can help you with:

  • Indication selection
  • Clinical trial design
  • Synopsis redaction
  • Ethical committee presentation
  • Clinical trial performance
  • Reporting
  • Efficacy and safety tests
  • Biomarkers
  • Hormonal modifications
  • Metabolism (PK, PD)
  • Biostatistics

Contact [info@b2h.be] us to discuss how these capabilities can forward your projects! We will help you develop tailored solutions.

Bio-analysis

  • Standard bio-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

For more information, click here.

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In addition, we manage API bulk reception, drug formulation and release. For more information, click here.

For your cell therapy requirements, you can click here to find out more about our CHU-LTCG facility on ATMP production in GMP conditions.

Contact [info@b2h.be] us to discuss how these capabilities can forward your projects! We will help you develop tailored solutions.