About QInscribe

AI-Driven Solutions for Regulatory Medical Writing

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

QInscribe is a specialist AI Medical Writing Contract Organisation that uses cutting-edge AI technology to generate regulatory documents that bring market leading speeds to the medical writing industry.

Our AI solutions generate 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 unique AI-driven approach brings new efficiencies that guarantees competitive pricing in the evolving medical writing space.

Why Choose QInscribe?

Designed for Agility

We combine clinical insight and AI technology 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 AI tools 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.