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Draft a Full Protocol Before Lunch?
Jul 4, 2025 | Document Management
Drafting a clinical trial protocol is rarely a swift process. Traditionally, it can take weeks or months of manual effort, version wrangling, and multi-stakeholder input before a trial is even close to starting. But a quiet revolution is underway in clinical...
Draft a Full Protocol Before Lunch?
Jul 4, 2025 | Document Management
Drafting a clinical trial protocol is rarely a swift process. Traditionally, it can take weeks or months of manual effort, version wrangling, and multi-stakeholder input before a trial is even close to starting. But a quiet revolution is underway in clinical...
Will Generative AI Outperform Your Best Medical Writer? The Data Says Yes—And No
Jun 13, 2025 | Artificial Intelligence
Benchmarking real-world accuracy, speed and compliance when large-language-models go head-to-head with human expertise. The Stakes: Why the Debate Matters for Clinical-Trial Documentation Clinical research lives and dies by its paperwork. From the first synopsis of a...
Improving Inefficiencies in UK Clinical Trial Units
May 13, 2025 | Innovation, Insights
Explore the Paper UK CTUs InefficienciesDownload Clinical Trials Units (CTUs) in the UK play a pivotal role in translating scientific concepts into safely conducted studies. Yet many CTUs still struggle with operational bottlenecks that slow study start-up and erode...
Using Smart Templates to Eliminate Manual Errors in Clinical Trial Documents
May 13, 2025 | Momentum, Technology
Manual drafting of clinical trial documents is notoriously time-consuming and prone to inconsistencies. A survey of UK Clinical Trials Units highlighted that document preparation often becomes a bottleneck, with parallel drafting of protocols, participant information...
Precision at Pace: Helping a Medical Writing Firm Streamline Protocol Development
Apr 18, 2025 | Case Studies
Protocol writing is the backbone of clinical research documentation. Every clinical trial begins with a protocol—a definitive guide that outlines the study’s rationale, design, procedures, and regulatory framework. Medical writing firms, particularly smaller ones, are...
Spotlight
Draft a Full Protocol Before Lunch?
Will Generative AI Outperform Your Best Medical Writer? The Data Says Yes—And No
Improving Inefficiencies in UK Clinical Trial Units
Using Smart Templates to Eliminate Manual Errors in Clinical Trial Documents
Precision at Pace: Helping a Medical Writing Firm Streamline Protocol Development
Rethinking Protocol Digitalisation: Strength in Structure, Speed in Execution
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Precision at Pace: Helping a Medical Writing Firm Streamline Protocol Development
Apr 18, 2025
Protocol writing is the backbone of clinical research documentation. Every clinical trial begins with a protocol—a definitive guide that outlines the study’s rationale, design, procedures, and regulatory framework. Medical writing firms, particularly smaller ones, are...
From Months to Days: How Automation Transforms Clinical Trial Protocol Efficiency
Nov 29, 2024
The High Stakes of Clinical Trial Protocol Development Clinical trials play a critical role in advancing healthcare by bringing new treatments and interventions to patients. Central to these trials is the protocol—a comprehensive document detailing the study’s design,...
Momentum transforms how protocols are written and amendments are managed — replacing manual effort with automation, accuracy, and speed. From set-up to submission, everything starts working smarter.
Your protocol delivered faster than your morning coffee
Populate your trial details once and generate a fully formatted, submission-ready protocol in a few minutes. No templates to wrangle, no tables to align, no consistency checks.Â
One change. Every document. Instantly.
Explore how Momentum helps you handle protocol changes, site-level updates, and regulatory amendments in minutes — not weeks. One change, reflected everywhere. Discover how it works.