Say goodbye to

manual

time-consuming

tedious

manual

time-consuming

tedious

manual

time-consuming

tedious

manual

regulatory & medical writing

Managing complex regulatory documentation – is anything but simple.

Whether building a CTD, drafting a CSR, or preparing PSURs, the challenges are the same: long turnaround times, high costs, compliance risks, and pressure to do more with less. Manual work doesn’t scale, leading to delays, missed deadlines, and lost revenue.

Whether building a CTD, drafting a CSR, or preparing PSURs, the challenges are the same: long turnaround times, high costs, compliance risks, and pressure to do more with less.

Save time for your medical and regulatory teams!

Book a Demo

The fastest way to generate
compliant regulatory documentation

From data extraction to final draft, Syntro transforms fragmented workflows into one smart, unified system for faster, easier submissions.

Periodic Safety Update Reports (PSURs)
Development Safety Update Reports (DSURs)
eCDT Module 2.5
eCDT Module 5
Literature Reviews and Reference Listings
Risk Management Plan (RMP)

The document you work on is missing?

Let us know what you need

Designed for the complexity
of live sciences documentation

Syntro isn’t just about faster documents. It’s about transforming how pharma and CROs create, manage, and deliver compliant content.

Smart literature search

Quickly find, filter, and extract the right data from scientific publications and public sources – no more hours wasted digging.

Automated drafting

Generate structured, submission-ready content faster than ever.

Deep research assistant

Ask any scientific question – get accurate, source-backed answers in seconds.

Source traceability

Track every AI-generated output back to its original source instantly.

Built-in regulatory intelligence

Stay aligned with EMA, FDA, and ICH guidelines automatically, as you write.

and so much more on the way!

Move faster. Work smarter.
Stay compliant.

Move faster.
Work smarter.
Stay compliant.

From faster submissions to lower costs and audit-ready documents – Syntro gives you measurable impact from day one.

Accelerate your submissions

Cut your IND, NDA, or CTA timelines by up to 5 times – without sacrificing quality or compliance.

Reduce manual work

Accelerate your submissions

Automate the most time-consuming tasks – literature review, data extraction, formatting – to lift the burden from your team, so they can focus on strategy, not grunt work.

Lower your costs

Accelerate your submissions

Avoid hundreds of thousands spent drafting the same documents from scratch.

Work with confidence

Accelerate your submissions

Trust the output – zero hallucinations means your team doesn’t waste time fact-checking or fixing misleading content.

Be ready for audits

Accelerate your submissions

Ensure instant compliance with EMA and FDA guidelines, so your documentation is submission‑ready from day one.

Effectiveness backed
by numbers

2440+

Hours saved for regulatory and medical writing teams

145

Drafts created

90%

Accuracy

Halucinations

Learn more about Syntro

Your standards, our priority – secure, compliant data management in close cooperation with your legal and IT teams.

Your standards, our priority – secure, compliant data management in close cooperation with your legal and IT teams.

Your standards, our priority – secure, compliant data management in close cooperation with you legal and IT teams.

Integrations

Our platform integrates seamlessly with tools like SharePoint, PubMed, and Veeva to ensure smooth data flow and minimal disruption.

Security

Syntro is built with advanced security features to protect your data, ensuring confidentiality and preventing unauthorized access.

Legal

We uphold the highest legal standards, ensuring that your data is handled responsibly and in full compliance with international regulations.

Collaborating across disciplines
to revolutionize regulatory writing

Our mission is to change the way medical and regulatory writers handle documentation.

Agata

CEO

Top female leader with a foundation in VC and molecular biology.

Joanna

Sales & marketing

12 years’ science expertise in sales, communication and medical writing.

Mateusz

CTO

Brilliant mathematician and AI expert, with
a background at Nvidia.

Brilliant mathematician and AI expert, with a background at Nvidia.

Szymon

Software development

Fullstack with 8 years of experience, previously at Ramp.

Paweł

UX & Design

UX design expert with a portfolio of top banking & fintech projects

Anna

Medical Writing QA

15 years of writing expertise for clients like Parexel.

Ready for Syntro?
Schedule a meeting

Request your personalized demo and discover how Syntro can transform your workflow.

Request your personalized demo and discover how Syntro can transform your workflow.

Still hesitant? We are here to help.
Reach us out

Still hesitant? We are here to help.

Request your personalized demo and discover how Syntro can transform your workflow.

Still hesitant? We are here to help.
Reach us out

Reach us out

Book a Demo

Book a demo

Say goodbye to

manual

time-consuming

tedious

manual

manual

time-consuming

tedious

manual

manual

time-consuming

tedious

manual

regulatory & medical writing

The fastest way to generate compliant regulatory documentation