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Improving Inefficiencies in UK Clinical Trial Units
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...
Improving Inefficiencies in UK Clinical Trial Units
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
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
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...
Rethinking Protocol Digitalisation: Strength in Structure, Speed in Execution
Introduction The clinical research industry is undergoing a quiet but significant transformation. For decades, the clinical trial protocol has existed as a static, monolithic document—written once, revised repeatedly, and copied manually into every system that depends...
The Rise of Decentralised and Virtual Clinical Trials: A New Era in Research
 clinical trials is undergoing a dramatic transformation. Traditionally, clinical trials have been site-based, requiring patients to visit hospitals or research centres regularly for monitoring, tests, and data collection. However, technological advancements,...
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Precision at Pace: Helping a Medical Writing Firm Streamline Protocol Development
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
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.
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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
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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.