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Monday 9am - 5:30pm Tuesday 9am - 5:30pm Wednesday 9am - 5:30pm Thursday 9am - 5:30pm Friday 9am - 5:30pm

QInscribe

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We are a specialist AI Medical Writing Contract Organisation that provides regulatory documents.

15/10/2026

🧾 Plain Language Summaries (PLS) are now mandatory under the EU Clinical Trials Regulation, and will be publicly available in the Clinical Trials Information System (CTIS).

In our latest guide, we cover:

✅ What a PLS is and how it differs from a scientific abstract
✅ EU CTR requirements and key timelines, including paediatric deadlines
✅ CTIS submission tips and common mistakes to avoid
✅ A strategic checklist to keep your summary neutral, clear and easy to read

Want to make sure your PLS is ready for CTIS the first time? Click here to read the blog: https://hubs.li/Q04ypZhP0

14/10/2026

What you gain by partnering with QInscribe 👇

✅ Confidence in regulatory submissions
Structured Clinical Study Reports (CSRs) that stand up to review.

✅ Faster turnaround without compromise
Experienced teams that deliver quickly without sacrificing on the quality.

✅ Less administrative burden
We handle planning, version control, and review coordination, to free up your time for other tasks.

✅ Clear, persuasive communication
We aim to clearly communicate what was planned, performed and observed.

✅ A scalable solution
One document, or an entire portfolio, our services flex around your needs.

To learn more about our medical writing services, enquire now:
https://hubs.li/Q04ypWdl0
Or email: [email protected]

Twitter Version:
Partner with QInscribe: ✅ Review-ready CSRs ✅ Fast turnaround (no quality trade-off) ✅ Less admin-planning, versions & reviews handled ✅ Clear reporting ✅ Scalable support.
Enquire: https://hubs.li/Q04ypWdl0 | [email protected]

13/10/2026

🏃‍➡️ Speed up your clinical study reporting without compromising quality.

At QInscribe, we’ve integrated generative AI into our workflow to slash CSR drafting times by up to 90%. But how does it work, and what does it mean for regulatory compliance and medical writing teams?

👆 Discover how our automated CSR generator is reshaping timelines and expectations across the industry: https://hubs.li/Q04ypYWW0

08/10/2026

👀 A second set of eyes can make all the difference.

Our Regulatory Writing services provide independent, expert review to catch any inconsistencies within your documents.

☑️ Get full confidence with a final check. Learn how our QC specialists can help you reduce risk and avoid delays: https://hubs.li/Q04ypVq20

07/10/2026

💼 Ensure your Clinical Study Report includes clear and well documented outcomes with Patient Safety Narratives.

Whatever the volume of safety narratives you require to be written, our automated approach enables us to handle large volumes at scale without compromising on quality.

🔎 Discover how we can support your clinical trial with well-written, efficient, and compliant narrative delivery: https://hubs.li/Q04ypVlc0

06/10/2026

🔒 Clear consent builds trust and protects your clinical trial.

We develop informed consent documents that are accurate, accessible, and aligned with global ethical and regulatory expectations. We support you so you can support participants with compassionate and patient-centric communication.

👆 Learn how we support compliant, patient-focused ICD development: https://hubs.li/Q04ypTj00

01/10/2026

🤖 Reduce the time to generate a first draft Clinical Study Report by 35-45% with QInscribe's AI-enabled CSRs.

We deliver CSRs that are clear, compliant, and submission-ready. Our AI tech assists in creating faster first drafts than ever before, coupled with the expertise you expect with human-in-the-loop review.

💻 Explore how we support high-quality CSR development at every phase: https://hubs.li/Q04ypRBX0

08/06/2026

🤔 What does AI mean for the future of medical writing?

From speeding up document creation to supporting compliance and consistency, AI is transforming how clinical and regulatory teams work. How do we strike the right balance of human-in-the-loop and AI advancements?

👆 Explore the evolving role of AI in medical writing in our blog: https://hubs.li/Q04jlHp00

05/06/2026

👍 Confident submissions start with exceptional writing.

Our AI-driven regulatory writing services are designed to minimise queries, meet global standards, and keep your timelines on track, whether you need a full submission package or targeted support.

⚡ Discover how we support smarter, faster submissions for your clinical trial: https://hubs.li/Q04jlMHv0

02/06/2026

🧾 Plain Language Summaries (PLS) are now mandatory under the EU Clinical Trials Regulation, and will be publicly available in the Clinical Trials Information System (CTIS).

In our latest guide, we cover:
✅ What a PLS is and how it differs from a scientific abstract
✅ EU CTR requirements and key timelines, including paediatric deadlines
✅ CTIS submission tips and common mistakes to avoid
✅ A strategic checklist to keep your summary neutral, clear and easy to read

Want to make sure your PLS is ready for CTIS the first time? Click here to read the blog: https://hubs.li/Q04jlGPK0

Address

Bevan House, 9-11 Bancroft Court
Hitchin
SG51LH

Opening Hours

Monday	9am - 5:30pm
Tuesday	9am - 5:30pm
Wednesday	9am - 5:30pm
Thursday	9am - 5:30pm
Friday	9am - 5:30pm

Telephone

+441462440084

Website

http://qinscribe.com/, https://www.linkedin.com/company/qinscribe/

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