Quanticate

Name: Quanticate
Address: Bevan House, Bancroft Court, Hitchin, SG51, GB
Telephone: +441462440084

Welcome to Quanticate's page. We are a leading global Clinical Research Organization (CRO).

Quanticate, with headquarters in the UK and USA, is a specialist Clinical Research Organization (CRO) primarily focused on the management, analysis and reporting of data from clinical trials and post-marketing surveillance. We provide very efficient outsourcing solutions for companies who need additional capacity or who want to outsource certain functions in their entirety. We deliver scalable on-site and off-site data management, statistical consultancy, statistical programming & analysis, medical writing and pharmacovigilance services. We also have a staff recruitment arm, "Quanticate People", to help Sponsors find all types of permanent and contract staff. Quanticate works closely with biotech, pharmaceutical and medical device companies and prides itself in being a seamless extension of its customers’ internal teams. Many of our customers choose Quanticate simply because they want to know that their data will be looked after by a specialist biometrics CRO. We offer that specific expertise and the attention necessary to properly manage, analyze and report valuable data. With a combination of on-shore and off-shore resources spanning four continents, Quanticate is renowned for its customer service, scalability and superior results.

15/10/2026

💉 Case Study: Accelerating Vaccine Development with Expert Programming

When the world faced unprecedented challenges, swift action and specialist expertise was essential. Discover how Quanticate's world-class programming team partnered with a top-tier pharmaceutical company in the rapid development of a COVID-19 vaccine.

In this case study, you'll learn how we:

🔹 Provided tailored and scalable programming solutions to meet critical deadlines.
🔹 Managed high-stakes environments with professionalism and precision.
🔹 Ensured exceptional quality and regulatory compliance at every stage.

📖 Read our full case study to see how our programming solutions, honed over 30 years of industry experience, can drive your critical projects forward: https://hubs.li/Q04ypzj00

14/10/2026

🏎️ Speed up your CSR generation with Quanticate's AI tools. 🤖

Utilise our automation systems to generate initial CSR drafts in as little as 15 minutes, reducing your time to deliverable while maintaining traceability and compliance.
By combining AI-generated outputs with our expert review, your drafts will be clear, consistent, and aligned with regulatory expectations.

Learn how you can streamline documentation for your clinical development teams.

🧭 Explore new AI capabilities. https://hubs.li/Q04ypwn20

13/10/2026

🤖 AI Advancements for Clinical Trial Design

Contemplating the usage of AI in designing your clinical trial? The burgeoning tech can help optimise protocols, improve patient recruitment, and accelerate timelines. With the right approach, AI-driven insights can even reduce costs and enhance trial success rates.

Our blog explores the different facets of AI within clinical trial design, such as:
🔹 How AI is reshaping trial design
🔹 Key benefits for sponsors and CROs
🔹 Challenges and regulatory considerations

Get it all in our blog below. ⬇️
https://hubs.li/Q04ypw7c0

08/10/2026

📢 Why R Programming is Changing Clinical Trial Analysis

Pharmaceutical and biotech companies are turning to R programming for data analysis and easy visualisations. As CROs adopt R programming into clinical workflows, understanding its role in clinical research is essential for data-driven decision-making and competitive advantage.

Our blog covers all the ways R programmaing is beneficial in clinical trial reporting, including:
🔹 How R is used in clinical trials 🧬
🔹 Key benefits over traditional statistical tools 💡
🔹 Regulatory considerations for using R in submissions 📜

Explore the full insights below. 🧠
https://hubs.li/Q04ypvYY0

07/10/2026

🏅 Set Your Clinical Trial up for Success with a well written SAP

A Statistical Analysis Plan (SAP) is essential for ensuring clarity and consistency in clinical trials, helping to reduce variability or odd results. A well-structured SAP defines analysis methods, avoids ambiguity, and streamlines regulatory submissions.

Our blog covers:
🔹What goes into a strong SAP 📝
🔹Best practices for creating a SAP 🔍
🔹Steps to ensure a submission-ready SAP 📑

Don't get stuck with a bad SAP. Read our blog below. 👇
https://hubs.li/Q04ypwc60

06/10/2026

When you're ready to begin the database lock (DBL) process, it means you're nearing the end of your data management process. What you include in your DBL is what will be presented to the FDA, which is why it's imperative to get it right. Any delays or errors at this stage can lead to regulatory setbacks and increased costs.

Our blog details different aspects of achieving a robust DBL, such as:
🔹 Why database lock matters 🗂️
🔹 Key steps for a seamless process ✅
🔹 Common pitfalls and how to avoid them ⚠️

A well-executed DBL keeps trials on track and ensures high-quality data submissions.

Ensure high-quality data submissions with a strong DBL. 💪
https://hubs.li/Q04ypvr60

01/10/2026

💡 Simplifying Macro Variables in SAS

Manually assigning macro variables in SAS creates tedious, unnecessary work. The INTO statement in PROC SQL automates this process, making your code cleaner, more efficient, and easier to maintain. If you work in clinical data programmaing or biostatistics, read our blog for everything you need to know about SAS automation.

We've included the following in our blog:
🔹 How the INTO statement works in PROC SQL 🛠️
🔹 Practical examples for creating macro variables dynamically 📊
🔹 Common mistakes to avoid when using this technique ⚠️

Learn how to streamline your SAS workflow below. 🔗
https://hubs.li/Q04yptN60

10/06/2026

📊 Case Study: Integrated Summary of Safety for Oncology Data Pooling

Oncology programmes often require safety data to be assessed across multiple studies, patient populations, and dosing contexts.

In this case study, discover how Quanticate supported a biopharmaceutical sponsor with:
🔹 Integrated Summary of Safety delivery across four clinical trials
🔹 Pooled analysis of treatment-emergent safety outcomes
🔹 Harmonised safety endpoints, PK/PD data, and monitoring outputs
🔹 Evidence-led insights to support clinical monitoring and dose evaluation

📖 Read the full case study:
https://hubs.li/Q04ks13_0

08/06/2026

💭 eCRF Design Best Practices

A poorly designed electronic Case Report Form (eCRF) can lead to data errors and delays, putting your study at risk. Getting it right from the start is key to a successful clinical trial. 💪

By creating an effective eCRF, you ensure accurate data collection, regulatory compliance, and streamlined workflows. We've explained the critical aspects of eCRF design in our blog, from structuring forms for usability to avoiding common pitfalls that can compromise data integrity.

Read our blog below:
https://hubs.li/Q04jlzz20

05/06/2026

📢 NEW PODCAST EPISODE: What is Clinical Data Review?

In this episode, Jullia and Tom explore clinical data review and why it plays a key role in study oversight, subject safety, and confident trial decision-making.

👂 Listen to the full podcast here: https://hubs.li/Q04jlNZF0

Address

Bevan House, Bancroft Court
Hitchin
SG51

Telephone

+441462440084

Website

http://www.quanticate.com/

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