Clinical Services

clinical servicesCROS NT can support Sponsors looking for clinical services to apply a full service approach when necessary. Our internal clinical experts can support with overall clinical strategy and development including the planning, design and execution of product development.

Early Phase Clinical Services (Phases I/IIa)

CROS NT can provide clinical and strategic product development advice and consultancy regarding study design and selection of suitably qualified Phase I units, including:

  • Protocol Development
  • Study Document Development
  • Study Monitoring
  • Medical Safety Monitoring
  • Bioequivalence/Bioavailability
  • Proof of Concept
  • Pharmacokinetics/Pharmacodynamics
  • First in Man
  • Safety & Tolerability
  • Special “population groups”

Late Phase Clinical Services (Phases IIb/III/IV)

clinical servicesWith our full range of clinical, regulatory and biometrics services, our clients gain end-to-end project planning to build quality into their clinical trials from the start – with mitigating risk strategies and efficient and effective time and budget planning.

CROS NT’s highly experienced clinical operations team provides strong site management and patient enrollment strategies based on well-researched evidence-based feasibility assessments. We utilize expert medical monitors to provide important oversight of safety during trials.