Study Management & Reporting

Home / Solutions / Clinical Solutions / Clinical Study Management & Reporting
Understand more about how our solutions can help you gain a competitive advantage

Build effective trial strategies with disclosure in mind

Understanding global clinical trial disclosure requirements can help you 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.

Healthcare professionals collaborating around a tablet device.

Manage your study with disclosure in mind

When managing a clinical trial it is essential to understand the requirements of various international organizations and the changing regulatory requirements. Citeline provides global visibility into disclosure regulations through our world-class suite of TrialScope solutions and services, 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.

Our insights publications can provide context and analysis behind the changing requirements and industry trends.

  • Monitor global disclosure regulations throughout the clinical life cycle
  • Plan site selection with transparency requirements in mind
  • Author your study documents to facilitate public disclosure, patient communication and redaction
  • Understand industry trends and stay abreast of changes in regulation

Relevant Products & Services

Sitetrove
Sitetrove
Identify the sites and investigators that will help propel your trial over the line. Sitetrove’s team of expert analysts curates data from over 60,000 sources, resulting in a database that boasts over 530,000 investigators and more than 190,000 clinical trial sites spanning 185 countries.
Key Benefits
  • Successfully conduct site and investigator selection
  • Inform successful country selection
  • Get direct access to our leading expert analysts
Trialtrove
Trialtrove
Comprehensive clinical trial data you can trust. Combining unmatched coverage of the clinical trial space with unparalleled detail and granularity, Trialtrove is the only resource you can rely on to help surface the insights that will inform your strategy and enable you to deliver successful trials that meet your objectives.
Key Benefits
  • Improve your protocol development
  • Understand competitor clinical strategies
  • Get direct access to our leading expert analysts
Trialscope Disclose
TrialScope Disclose
Accelerated clinical trial disclosure starts here. TrialScope Disclose keeps you ahead of changing regulations and evolving expectations, empowering you to maintain global disclosure compliance from a single, centralized platform.
Key Benefits
  • Improve speed and accuracy of submissions
  • Automate data entry and streamline processes
  • Re-use approved trial data across global registries
Speak to a specialist

A specialist is ready to speak to you regarding your interests and find the solutions that are right for you.

Professionals submitting a form to find out more about Citeline.
Citeline may contact you about relevant products, services and content. To opt out of these communications or to manage what you receive, please visit our Preference Center.

Your information will be used in accordance with our Privacy notice.

Thank you for your interest in Citeline. Your message has been submitted and our team will be in touch soon.