Clinical Trials Resource Kit

Find content including trackers, practice notes, state law surveys, checklists, and templates addressing some key concepts and considerations related to setting up and managing human subjects research and clinical trials for drugs and medical devices.

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Related Content

• Contract Research Organization Agreements
  Get insights into negotiating and drafting agreements between contract research organizations (CROs) and drug or medical device company sponsors of clinical trials.

• Clinical Trials (EU, UK)
  Understand the regulatory framework for clinical trials conducted in the United Kingdom.

• Informed Consent for Clinical Trials Form
  Draft an informed consent for clinical trials using this template.

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