Clinical Trial Registration & Result Disclosures

Stay compliant while freeing your team from admin.

You’re under pressure to deliver results. We make sure regulatory disclosures aren’t what slow you down. QInscribe takes this burden off your hands, giving you confidence that everything is handled accurately, on time, and in full compliance.

With increasing enforcement across the US and EU, including fines up to €250,000, we help you avoid compliance risks and reputational damage. More importantly, we give your team space to focus on what matters most: running your trials, hitting milestones, and getting closer to approval.

End-to-End Support You Can Rely On

From initial registration to final results posting, we manage the entire disclosure process for you. Our Registration & Result Disclosures services include:

Trial Registration
Accurate, timely registrations that meet all global requirements and submission deadlines.
Protocol Amendments & Updates
We manage ongoing updates, recruitment status, completion dates, and protocol changes, therefore keeping your records current.
Results Posting
We draft and submit your results within mandated timelines, avoiding delays and enforced action.
Document Redactions
Sensitive data redacted from protocols, SAPs, and other documents, therefore protecting privacy while meeting transparency rules.
Compliance Risk Reviews
We utilise both AI and expert medical writers to spot potential issues early and help you stay ahead of audits, inspections, and evolving guidelines.

What You Gain by Partnering with QInscribe

Confidence in Regulatory Submissions

We handle the complexity so you don’t have to navigate multiple registries, systems, and evolving disclosure rules.

Faster Turnaround Without Compromise

We keep you on schedule, avoiding last-minute scrambles to post results or update protocols.

Less Administrative Burden

We protect you from penalties, ensuring your disclosures meet FDA Final Rule, EU CTR, and ICMJE requirements.

Clear, Persuasive Communication

We give you peace of mind with expert oversight, risk assessments, and ongoing maintenance.

A Scalable Solution

We adapt to your systems, whether you use PharmaCM, your own SOPs, or need direct registry access.

Let’s take disclosure off your to-do list.

Get in touch to see how we can manage your trial registrations and results efficiently, accurately, and with full compliance.