TrialScope Disclosure Services provides hands-on expertise across protocol registration, results disclosure, plain language summaries, redaction, and advisory services.
Hands-on services from registration through results and participant-facing summaries
Disclosure professionals with deep regulatory knowledge and direct registry experience
Select the services you need and scale support as priorities and requirements change
Prepare, review, approve, publish, and maintain clinical trial registration data across relevant registries.
Prepare and submit accurate results information, supported by specialists who understand registry requirements and disclosure workflows.
Develop accessible summaries that communicate clinical trial information clearly to participants and the wider public.
Support the review and redaction of clinical documents before public disclosure, balancing transparency obligations with the protection of sensitive information.
Use advisory services and workshops to evaluate policies, improve workflows, and build more consistent disclosure practices across your organization.
Support for authoring, reviewing, approving, publishing, and maintaining clinical trial registration data
Specialist support to prepare, review, and submit clinical trial results and related documentation
Consulting, authoring, quality control, design, and publication support for participant-friendly communications
Targeted support for applicable EU CTIS and EudraCT activities, including relevant trial application and registration tasks
Review and preparation of clinical documents for public disclosure while protecting confidential information
Practical guidance to strengthen disclosure policies, processes, governance, and team capabilities
Our specialists combine regulatory knowledge with hands-on experience in disclosure processes, registries, and TrialScope solutions. Working as an extension of your team, they provide practical support tailored to your workload, operating model, and disclosure priorities.
Deep expertise across global disclosure regulations, registry requirements, and evolving compliance frameworks
Direct hands-on experience with ClinicalTrials.gov, EudraCT, CTIS, and other major global registries
Specialists who know TrialScope solutions inside out and can support your team throughout the disclosure lifecycle
Whether you need targeted help with a single registration or results submission, or broader ongoing support across your entire disclosure program, TrialScope Disclosure Services scales to match your needs.
Our specialists work as a true extension of your team, absorbing disclosure workload so your in-house resource can focus on higher-value activities without compromising quality or timeliness.
See how a dedicated Citeline lead writer integrated with a rare disease sponsor’s medical writing group and cross-functional teams to help them deliver on time.
With no dedicated disclosure team and few processes in place, a midsize biotech turned to Citeline for end-to-end project management, QC, and flexible writing support.
TrialScope Disclosure Services provide hands-on expert support across the clinical trial disclosure lifecycle — including protocol registration, results disclosure, plain language summaries, redaction, and advisory services. Sponsors can select the services they need and scale support as priorities and requirements change.
Our specialists have direct experience across major global registries including ClinicalTrials.gov, EudraCT, EU CTIS, and others. We support both registry-specific tasks and cross-registry disclosure programs.
Our plain language summary service covers program consulting and development, summary authoring, quality control, graphic design, and publication support — helping sponsors communicate clearly with participants while meeting regulatory transparency requirements.
Yes. Through our advisory services and tailored workshops, we work with sponsors to evaluate existing disclosure policies and workflows, identify gaps, and build more consistent, inspection-ready processes across the organization.
