Amarex understands that proper planning and choosing the appropriate clinical investigator is key to conducting an informed and successful trial.  To ensure an efficient study start up, we perform a comprehensive, customized, feasibility questionnaire that will provide the feedback that will help us provide our clients with a custom, site-specific enrollment strategy and site selection.

​Our services include:

  • Coordination of Regulatory Consultation Meetings

  • Identify Investigators 

  • Development of Protocol and Protocol Quality Review

  • Collecting Clinical Investigator Feedback

  • Customized Feasibility Questionnaires to Assess Capability and Availability

  • Site Selections - Developed Criteria and Qualifications

  • Identify Protocol Design Concerns

  • Enrollment Strategies

    • Establish Enrollment Rate Expectations

    • Site Specific Enrollment Tracking

    • Subject Recruitment Contingencies

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