About QInscribe – A Medical and Regulatory Writing CRO

Efficient and Cost-Effective Solutions for Regulatory Medical Writing

Ensuring regulatory and scientific excellence across all facets of medical writing.

QInscribe is a specialist Medical Writing Contract Research Organisation (CRO) that uses AI-assisted internal workflows to support efficient, cost effective, high-quality regulatory document delivery.

Our AI-assisted internal workflows support the preparation of the first draft and templates of key regulatory documents such as the clinical study report (CSR), which our experienced team of writers complete and QC with the highest standards as you would expect of expert medical writers. Our approach improves efficiency and supports competitive pricing in the evolving medical writing space.

Why Choose QInscribe?

Designed for Agility

We combine clinical insight and AI efficient processes with a focused, flexible approach to medical writing. Whether you need a single protocol or end-to-end programme support, we scale to fit your needs.

A True Extension of Your Team

We work in close partnership with sponsors, seamlessly integrating with your internal workflows to reduce strain and improve efficiency. You can count on us to meet your standards and your timelines every time.

Specialists, Not Generalists

Writing is our craft, not an add-on. Our team includes dedicated writers, QC reviewers, and publishing experts who have experience across a broad range of therapeutic areas. Our team have worked exclusively on documentation, bringing clarity, compliance, and consistency to every deliverable.

Reduced Timelines & Lower Costs

The reason we have invested in the development of our internal AI capabilities isn’t just to benefit our own processes and streamline timelines, it’s so we can generate quality, finalised regulatory documents in record time. This enables us to reduce our rates and pass on the savings to our clients, while also increasing our own capacity to handle high volumes of deliverables.

Consistent High Quality

Quality is a standard embedded in every stage of our process. Whether we’re delivering a single protocol or a full suite of regulatory documents, our rigorous review procedures, specialist expertise, and commitment to compliance ensure consistently high standards. No matter the project size or scope, our clients can rely on clear, accurate, and regulator-ready deliverables every time.

What we do

We provide flexible, scalable support for medical writing, regulatory submissions, and transparency services, so you can stay focused on your science while we take care of the documentation.