Pricing
Built for investigators, & small to large trial teams
Clinical trials shouldn’t be limited by bureaucracy, budgets, or bloated processes. Whether you’re a seasoned academic investigator or part of a small trial team preparing your first study, Momentum brings the power of clinical trial automation right to your fingertips.
You no longer need to be part of a large CTU or CRO to benefit from automation. Momentum is now accessible to individual researchers, lone PIs, and compact study teams—without compromise.
Draft your protocol, streamline your documents, and launch with confidence. All from one secure, cloud-based platform.
All inclusive plans - Every Feature, Every Time
Whether you’re drafting your first protocol or managing a portfolio of studies, every Momentum plan comes with full access to our core platform. No feature gating. No half-access. Everything you need to get your trial off the ground—fast.
-
The full power of our clinical trial smart document generator
-
Centralised data entry with automatic syncing across documents
-
AI-powered assistance to help accelerate form filling
-
Pre-filled sponsor language and templated boilerplate text
-
Full amendment engine with unlimited amendments
No watered-down experience. No artificial restrictions.
investigator
Suitable for small trial teams, sole investigators, or small CROs, sponsors, and medical writers.
Enterprise
Suitable for CROs, trial teams, medical writring firms, sponsors, pharmaceutical companies.
TESTIMONIALS
Don't take it from us - here's what some other customers are saying about working with Momentum.
“I’m a PhD student preparing my first protocol.”
"I’d never written a full protocol before and was honestly overwhelmed by where to start. Momentum guided me through every section—from eligibility criteria to safety reporting—without needing to spend hours hunting down examples. What would have taken me weeks was drafted in just two days. It gave me the confidence to submit to ethics with a clear, professional protocol."
— Jasdeep K., PhD Candidate, University of Birmingham
“We’re a small biotech preparing our first submission.”
"As a team of three with no in-house medical writer, we needed a solution that didn’t slow us down. Momentum helped us generate the full IRAS package—protocol, PIS, GP letters, even our site templates—without needing to outsource. The consistency and audit trails made our sponsor review seamless. We couldn’t believe how quickly it all came together."
— Tom L., COO, Virexen Biotherapeutics
YOU MIGHT BE INTERESTED IN
Stay Ahead of the Curve
Explore our latest thinking on clinical trial innovation, operational challenges, and the future of documentation. From blog insights to white papers — it's all in our Resources hub.