Study conduct expertise

Depending on the available bed and resource capacity, we are able to initiate studies at short notice, manage additional unscheduled groups in active studies or arrange study postponements. For individual studies, unit space is booked on a “first come, first served” principal based on studies award time.

Occasionally, we receive short-term requests to pick up and expedite groups or to initiate new studies. In these cases, the variable bed capacity of our sites gives us flexibility in planning studies and dealing with unexpected bottlenecks.

List of our study expertise:

  • First-in-Man Trials
  • Proof-of-concept
  • Food effect
  • Drug-Drug interaction
  • Biosimilar/Bioequivalence
  • Long confinement
  • Various routs of administration (oral dosing, infusion, inhalation, intramuscular, intravenous, subcutaneous, topical etc.)
  • Safety and tolerability
  • Intensive safety monitoring
  • Cardiac monitoring in patients
  • Genotyping
  • Large healthy cohorts
  • Special patient populations

Our staff has experience in administering investigational medicinal products (IMPs) by all common routes of administration (oral, inhalative, intramuscular, subcutaneous and intravenous, topical, etc.). The so-called "Dosing Team" and our pharmacist know how important it is to prepare and administer the IMP exactly as stated in the protocol.