Trial disclosure doesn’t need to be stressful. Let us do the heavy lifting.

Nobody said disclosure was easy. Resources are stretched thin, rules are complex, and data sets span different registries and requirements. So let our team be your team. Our veteran disclosure experts work as an extension of your own staff. We do it all, from protocol registration through results posting.

And because we use the TrialScope Disclose™ platform, you don’t have to worry about costly manual errors or inefficiencies — and our services can flexibly scale to meet your organization’s unique needs.

What our team can do for you:

Properly register your trials with

Our team of experts will author, review, edit, approve and publish your protocol registrations and submission of clinical trial applications to global registries including, EudraCT, South Africa, Australia/New Zealand and others. From resolving comments, to ongoing maintenance, we take care of it all so you’re always up to date and fully compliant.

Manage your results disclosure

Once your trial results are in, we make sure they’re shared with the public in a transparent and timely manner. We prepare your study documents including: final study protocol, final statistical analysis plan (SAP) and amendments, disclosure on, and preparation of XML upload for EU trials.

Create your Plain-Language Summaries (PLS)

Sharing your trial results in simple language is a crucial part of transparency. We author your trial’s plain-language summary and post it to the portal for public access. We offer language translation and graphic design services too — and provide summaries for local affiliates as needed.

Prepare all redactions

Our team knows how to prepare and share clinical trial data while maintaining patient confidentiality. From developing rule sets, to redacting and anonymizing full submissions, to preparing or amending additional documents, we ensure that you and your patients are protected during all disclosure activities.

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Put our experts at your service.

Our disclosure experts ensure full global compliance and proactive transparency for all your clinical trials — so you don’t have to.