CLINICAL TRIALS SERVICES

Our Service Package

• Determining the scope of the trials (i.e. number of variables to evaluate)


• Identification of target population


• Identifying the number of patients required


• Randomization of the patients


• Determination of baseline levels of variables


• Protocol to meet Health Canada, FDA, and ICH guidelines


• Amount of time and costs associated with each phase of the Trials


• Selection of patients


• Selection of central lab


• Selection of evaluator


• Collection of safety and efficacy data


• Selection and auditing of the clinical research organization (CRO)


• Selection of indemnity insurance


• Database management


• Compile the submission
  
  
  

Assistance with Obtaining Funding

If required, we can help identify sources of public and/or private funding to help offset the costs of these Clinical Trials.