Study Management & Reporting

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Optimize site selection and protocol structure

Understanding global clinical trial disclosure requirements can help you to refine site selection and change the protocol structure. Protocols written with disclosure in mind avoid unnecessary sharing of sensitive information, reduce redaction costs and incorporate plain language elements to meet regulatory requirements and support patient engagement initiatives.

Regulatory study management and reporting

Plan your study with disclosure in mind

Citeline provides global visibility into disclosure regulations through our TrialScope Intelligence solution, allowing sponsors to refine their regulatory strategy and transparency plans. Our specialized medical writers can write your study documents to manage the scope and efficiency of public disclosure, reduce the cost of redaction and anonymization and support patient engagement initiatives.

  • Monitor global disclosure regulations throughout the clinical lifecycle
  • Plan site selection with transparency requirements in mind 
  • Author your study documents to facilitate public disclosure, patient communication and redaction
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