Quanticate

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.

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

03/06/2026

🌟 Optimising Early Phase Clinical Trials with BOIN Design 🌟

Discover the statistical benefits and practical applicability of Bayesian Optimal Interval (BOIN) designs. This method adapts dose levels based on patient responses, ensuring optimal balance between safety and efficacy. Compared to the traditional 3+3 design, BOIN offers enhanced precision, flexibility, and patient safety.

Interested in learning more about how BOIN can transform your clinical trials? Check out our blog here 👉 https://hubs.li/Q04jlNgC0

01/06/2026

Design of Phase I Oncology Studies 🌐

Understand the ins and outs of designing dose-finding oncology studies in our whitepaper that covers:

🚧 The challenges of oncology clinical trials design
💊 Maximum Tolerated Dose (MTD) and Dose-Limiting Toxicity (DLT)
📊 Model-based and Rule-based Designs
🧩 Why to use Model-based or Rule-based Designs
⚠️ Limitations of using Model-based Designs

Download our whitepaper to learn more ⬇️
https://hubs.li/Q04jlJcc0

29/05/2026

🎙️ QCast Episode 45: Clinical Trial Management Systems (CTMS)

In this episode, Jullia and Tom discuss clinical trial management systems and their role in keeping clinical studies under control.

👂 Listen to the full podcast here: https://hubs.li/Q04gBYtr0

27/05/2026

🧩 Streamline SDTM dataset creation with Quanticate’s automation tools.

Preparing SDTM datasets can be time-intensive, especially when consistency, traceability, and submission readiness are essential. Quanticate’s SDTM automation helps reduce manual effort while supporting high-quality, standards-aligned outputs.

Our approach supports:
🔹 Faster SDTM dataset generation
🔹 Consistent mapping across studies
🔹 Improved traceability from source to submission
🔹 Expert review from experienced clinical programmers

Build submission-ready SDTM outputs with greater efficiency and confidence.

⚙️ Explore SDTM automation: https://hubs.li/Q04gBQbq0

25/05/2026

📋 Accelerate tables and listings delivery with Quanticate’s automation tools.

Manual table and listing generation can slow down clinical reporting and increase the risk of inconsistencies. Quanticate’s automated tables and listings help streamline the creation of clinical reporting outputs while maintaining quality, traceability, and regulatory alignment.

Our tools support:
🔹 Faster generation of standard tables and listings
🔹 Consistent formatting across studies and submissions
🔹 Reduced manual rework for programming teams
🔹 Expert review from experienced statistical programmers

Improve reporting efficiency without compromising confidence in your outputs.

⚙️ Explore tables and listings automation: https://hubs.li/Q04gBFCH0

22/05/2026

📢 NEW PODCAST EPISODE: Clinical Trial Simulation

In this episode, Jullia and Tom explore clinical trial simulation and how it supports better study design decisions before a trial begins.

👂 Listen to the full podcast here: https://hubs.li/Q04gDyQt0

20/05/2026

⚡ Create repeatable, compliant Phase I workflows with Quanticate.

Quanticate’s Phase I Standardisations help emerging biotechs and Phase I units streamline study setup, reduce avoidable variability, and improve consistency across early-phase programmes.

Our framework supports:
🔹 Faster setup for repeatable studies
🔹 Alignment with CDISC or sponsor-specific standards
🔹 Reusable workflows across similar programmes
🔹 Greater confidence in data quality and regulatory readiness

Build a more predictable path from raw data to analysis-ready outputs.

🧭 Explore Phase I Standardisations: https://hubs.li/Q04gCHgM0

Address

Bevan House, Bancroft Court
Hitchin
SG51

Telephone

+441462440084

Website

http://www.quanticate.com/

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