Bioequivalence

 

 
 
Shandon Clinic was initially formed as a bioequivalence unit catering to the generics industry. The resources within the clinic are set up to provide our clients with a “full service”, from initial study design through to final integrated study report.

Our key strengths include:

  • Experience (more than 300 BE studies completed)
  • Quality (praised by regulators and auditors alike)
  • Speed (rapid turnaround once approvals obtained)
  • Technical expertise (associate laboratories are A-listed)
  • Personal management of studies by senior staff throughout
  • Expert consultancy prior to study start (strategy, design) and after study completion (regulatory questions) as standard
  • Cost-effective (low priced by European / US standards)
  • Excellent reputation throughout Europe and beyond


We have an extremely high incidence of repeat business. Clients state that they particularly value the rapid responsiveness of senior staff at Shandon Clinic, and the “hands-on” management of their projects by experienced researchers.

Shandon Clinic has recently expanded. Clinical units in South Africa and Turkey now afford us increased capacity, and allow provision of cost-effective service to clients who have difficulty meeting the requirements imposed by the EU Clinical Trials Directive.

Other Principal Servcies include:

Recently completed and ongoing studies can be reviewed in our News page.

 

 
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