What are the opening hours?

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

QInscribe

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

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

29/05/2026

🤔 Explaining key elements of your clinical trial in non-technical language that the general public can understand is a regulatory requirement.

Plain Language Summaries, AKA Lay Summaries, meet these requirements and help you communicate your trial results with transparency and accuracy.

🏋️ Support disclosure and stay complaint. See how we make your complex trial accessible and audit-ready: https://hubs.li/Q04gNZq00

26/05/2026

📘 Investigator’s Brochure (IB) is more than a box-ticking document — it is the living “source of truth” for safe dosing, monitoring, and informed trial conduct.

In our latest guide, we break down:

✅ What an IB is (and why it matters under modern GCP expectations)
✅ The core sections along with what “good” looks like in practice
✅ Version control, annual review cycles, and out-of-cycle safety updates
✅ The EU/UK perspective on Reference Safety Information (RSI) and expectedness

👆 If you’re building or updating an IB for your next study, this is a practical checklist to bookmark: https://hubs.li/Q04gP6nX0

21/05/2026

🚹 Anonymisation done right means less risk and fewer hang-ups with your clinical data and documents.

Our expert-led anonymisation services help you meet global transparency requirements while protecting participant privacy and commercial integrity.

Make sure your clinical data and regulatory documents are submission-ready and audit-proof.

👆 Anonymise your clinical data and documents here: https://hubs.li/Q04gP1330

18/05/2026

🏃‍➡️ 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/Q04gNLc80

24/04/2026

🏆 High-quality medical writing doesn’t happen by accident.

Quality control and scientific review are essential to ensuring regulatory documents are accurate, compliant, and fit for submission. But what does a robust review process look like? And how can it help avoid costly delays?

👆 Our blog has the answers. https://hubs.li/Q04cSgZX0

21/04/2026

📋 Why SOPs are critical in clinical trials

Standard Operating Procedures (SOPs) provide the structure needed to ensure consistency, compliance, and quality across every stage of a clinical trial.

This blog explores:
🔹 What SOPs are and why they matter
🔹 Key components of effective SOPs
🔹 How they support regulatory compliance and operational efficiency

📖 Read the full blog:
https://hubs.li/Q04blbJk0

17/04/2026

🔒 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/Q049Pddv0

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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