Clinical Trial Transparency Services
Protect patient data amidst changing regulations
Global expectations around trial disclosure and public data sharing are rising. At QInscribe, we help you meet complex transparency requirements without overburdening your internal teams. From plain language summaries to anonymisation strategies, our tailored services support regulatory compliance and public engagement across every stage of development.
Whether you’re responding to EU CTR requirements, ClinicalTrials.gov timelines, or industry best practices, we provide clear, consistent, and regulation-ready outputs that reduce pressure and protect your programme.
Our Clinical Trial Transparency Services Include:
Registration & Result Disclosures
Timely and compliant registration and result posting to global public registries, such as ClinicalTrials.gov & EU CTR Submissions, EudraCT, ISRCTN, and other global platforms. Read more.
Data & Document Anonymisation
Protect sensitive data while meeting disclosure obligations under policies such as EMA Policy 0070, Health Canada PRCI, and other global transparency guidelines. Read more.
Plain Language Summaries
Lay summaries that translate complex results into accessible language, meeting regulatory and ethical obligations across the EU and global frameworks. Read more.
What You Gain by Partnering with QInscribe
Compliant by Design
Our processes are aligned with evolving global regulations, including EMA, Health Canada, and ClinicalTrials.gov standards, so your team stays ahead of disclosure timelines.
Patient-Centric Communication
We craft summaries that support public understanding, patient trust, and ethical transparency, without sacrificing scientific accuracy.
Data Protection You Can Rely On
From redaction to anonymisation, we help you share what’s required while protecting what matters: confidential data, commercial integrity, and participant privacy.
We’ll help you deliver with confidence.
Contact us to explore how we can support your clinical trial transparency strategy efficiently, accurately, and with full compliance.