Quanticate

Call Directions Website Contact the business

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: 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:
πŸ”Ή Early-phase trial design and biometrics expertise
πŸ”Ή Flexible support tailored to evolving study needs
πŸ”Ή High-quality data delivery to support critical decisions

πŸ“– 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.

πŸƒ Accelerate your SAP development without compromising quality using Quanticate's AI tools. πŸ€–Quanticate's AI technology ...
21/10/2026

πŸƒ Accelerate your SAP development without compromising quality using Quanticate's AI tools. πŸ€–

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:
πŸ”Ή Section-specific statistical methods
πŸ”Ή Traceable links to your protocol specifications
πŸ”Ή 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

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

πŸ“‹ 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:
πŸ”Ή Seamless amendment integration and cross-team communication
πŸ”Ή Quick deliverable turnaround due to automated SMC listings
πŸ”Ή Inspection-ready data delivered on schedule to regulatory authorities

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

πŸ’‰ Case Study: Accelerating Vaccine Development with Expert ProgrammingWhen the world faced unprecedented challenges, swi...
15/10/2026

πŸ’‰ 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:

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

πŸ“– 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. πŸ€–Utilise our automation systems to generate initial CSR draf...
14/10/2026

🏎️ Speed up your CSR generation with Quanticate's AI tools. πŸ€–

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

πŸ€– AI Advancements for Clinical Trial Design Contemplating the usage of AI in designing your clinical trial? The burgeoni...
13/10/2026

πŸ€– 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:
πŸ”Ή How AI is reshaping trial design
πŸ”Ή Key benefits for sponsors and CROs
πŸ”Ή Challenges and regulatory considerations

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

πŸ“’ Why R Programming is Changing Clinical Trial AnalysisPharmaceutical and biotech companies are turning to R programming...
08/10/2026

πŸ“’ 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:
πŸ”Ή How R is used in clinical trials 🧬
πŸ”Ή Key benefits over traditional statistical tools πŸ’‘
πŸ”Ή Regulatory considerations for using R in submissions πŸ“œ

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

πŸ… Set Your Clinical Trial up for Success with a well written SAPA Statistical Analysis Plan (SAP) is essential for ensur...
07/10/2026

πŸ… 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:
πŸ”ΉWhat goes into a strong SAP πŸ“
πŸ”ΉBest practices for creating a SAP πŸ”
πŸ”ΉSteps to ensure a submission-ready SAP πŸ“‘

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

When you're ready to begin the database lock (DBL) process, it means you're nearing the end of your data management proc...
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:
πŸ”Ή Why database lock matters πŸ—‚οΈ
πŸ”Ή Key steps for a seamless process βœ…
πŸ”Ή 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. πŸ’ͺ
https://hubs.li/Q04ypvr60

Address

Bevan House, Bancroft Court
Hitchin
SG51

Alerts

Be the first to know and let us send you an email when Quanticate posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Business

Send a message to Quanticate:

Shortcuts

Share