Quanticate

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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.

🌍 Case Study: Decentralised Phase 3 Dermatology StudyDecentralised trials bring flexibility and patient accessibility, b...
29/10/2026

🌍 Case Study: Decentralised Phase 3 Dermatology Study

Decentralised trials bring flexibility and patient accessibility, but also introduce new operational and data challenges.

In this case study, discover how Quanticate supported a Phase 3 dermatology study with:
🔹 Decentralised trial design and ex*****on
🔹 Integrated data management and biometrics support
🔹 Efficient delivery in a complex, patient-centric setting

📖 Read the full case study:
https://hubs.li/Q04ypMkt0

⚡ Create repeatable, compliant Phase I workflows with Quanticate.Quanticate’s Phase I Standardisations help emerging bio...
28/10/2026

⚡ 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/Q04ypy9s0

🧬 Case Study: Phase I Dose Escalation in Oncology TrialsDose escalation studies are critical in early-phase oncology, bu...
27/10/2026

🧬 Case Study: Phase I Dose Escalation in Oncology Trials

Dose escalation studies are critical in early-phase oncology, but require careful design and ex*****on to balance safety and efficiency.

In this case study, see how Quanticate supported a sponsor with:
🔹 Dose escalation strategy and trial design
🔹 Statistical and programming expertise
🔹 Data-driven insights to guide decision-making

📖 Read the full case study:
https://hubs.li/Q04ypJQs0

🧬 Case Study: Supporting Early-Phase Oncology Gene Therapy TrialsEarly-phase oncology studies come with unique challenge...
22/10/2026

🧬 Case Study: Supporting Early-Phase Oncology Gene Therapy Trials

Early-phase oncology studies come with unique challenges, especially in complex areas like gene therapy.

In this case study, discover how Quanticate supported a sponsor with:
🔹 Early-phase trial design and biometrics expertise
🔹 Flexible support tailored to evolving study needs
🔹 High-quality data delivery to support critical decisions

📖 Read the full case study:
https://hubs.li/Q04ypDrx0

Quanticate welcomes Praveen Arockiaraj as VP and Head of Clinical Data Management.With more than 22 years of experience ...
21/10/2026

Quanticate welcomes Praveen Arockiaraj as VP and Head of Clinical Data Management.

With more than 22 years of experience across global CRO and pharmaceutical environments, Praveen brings extensive expertise in Clinical Data Management, global team leadership and operational excellence.

In his new role, he will lead Quanticate’s global Clinical Data Management group, supporting continued growth, data integrity and the delivery of high-quality clinical data services.

Please join us in welcoming Praveen to Quanticate.

Read the announcement: https://hubs.li/Q04BT2WG0

Quanticate appoints Praveen Arockiaraj as VP and Head of Clinical Data Management, bringing over 22 years of clinical research and data management experience.

🏃 Accelerate your SAP development without compromising quality using Quanticate's AI tools. 🤖Quanticate's AI technology ...
21/10/2026

🏃 Accelerate your SAP development without compromising quality using Quanticate's AI tools. 🤖

Quanticate's AI technology searches through your structured protocol content and metadata to generate draft Phase I SAPs, fully aligned with your internal templates.
This Python-based system builds:
🔹 Section-specific statistical methods
🔹 Traceable links to your protocol specifications
🔹 Accurate, metadata-driven narratives

Your final SAPs are reviewed and refined by experienced biostatisticians, combining automation with scientific oversight.

⚡ Fast-track your SAP. https://hubs.li/Q04ypwFN0

📋 Case Study: ABC Oncology Trial Safety Monitoring Committees (SMC)When biotechs are pressured to meet tight timelines f...
20/10/2026

📋 Case Study: ABC Oncology Trial Safety Monitoring Committees (SMC)

When biotechs are pressured to meet tight timelines for regulatory approval, it's important to have the right CRO to support your team and processes. See how we scaled to support our biotech sponsor by providing clinical data management services and SMC creation.

Key outcomes:
🔹 Seamless amendment integration and cross-team communication
🔹 Quick deliverable turnaround due to automated SMC listings
🔹 Inspection-ready data delivered on schedule to regulatory authorities

Read the full case study here: https://hubs.li/Q04ypCT20

💉 Case Study: Accelerating Vaccine Development with Expert ProgrammingWhen the world faced unprecedented challenges, swi...
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

🏎️ Speed up your CSR generation with Quanticate's AI tools. 🤖Utilise our automation systems to generate initial CSR draf...
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

🤖 AI Advancements for Clinical Trial Design Contemplating the usage of AI in designing your clinical trial? The burgeoni...
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

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