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.
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.
