Site Selection & Trial Startup RegPharmaClin

Site Selection & Trial Startup

How it works

Strategically selecting the right sites to conduct clinical trials is essential to ensure the success of a trial. I have extensive therapeutic specific site knowledge and experience with sites across Europe and dedicated units with local site knowledge manage.

Qualified staff provide expertise in submission, follow-up and authorization processes in compliance with local and international regulations and guidelines

Startup activities include:

  • Country and Site Feasibility
  • Site Selection
  • Preparation of submission package
  • Submissions to IEC/IRB and follow-up
  • Review, prepare and negotiate the contracts and budgets
  • Ensure final ethics approval are granted
  • Ensure the contracts are fully executed

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