Services - Clinical Research

Shandon are committed to providing reliable information for our clients as well as protecting the participants of clinical trials. Our protocols ensure compliance with ICH Good Clinical Practice and all trial's at Shandon Clinic deliver qualified data for our clients across our portfolio of services. Services include:

 
protocol and case record form development
IRB and Irish Medicines Board submissions
recruitment and screening
clinical phase
data management and statistical analysis
clinical report writing
 
Clinical Trials include:
Bioequivalence testing
Pharmacokinetics studies
Out-patient studies (Phase II - IV)
Other Services
   

Analysis of plasma samples is generally arranged with one of our associate laboratories. Recent lists of validated methods are available on request.

 

 

  
 
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