Quanticate

At Quanticate, our approach to statistical programming is built on a foundation of specialist expertise paired with industry-leading automation and tools. This combination allows us to handle complex datasets efficiently, ensuring high-quality results that are ready for regulatory submission. Our experienced global team of programmers work closely with clinical teams to implement automation where it adds the most value, reducing manual processes and minimising the risk of errors. The result is not only faster and more accurate data processing, but also the assurance that our expert oversight guarantees the highest level of data integrity throughout the study. For those seeking the best of both worlds, our statistical programming services delivers robust and reliable solutions by utilising our expert knowledge honed over 30 years in the industry, and our drive for technological innovation. To find out how we can tailor our solutions to your trials, click here to schedule a call with one of our specialists: https://hubs.li/Q02YvcWN0 #StatisticalProgramming #Automation #Expertise #CRO #DataIntegrity #Quanticate #ClinicalTrials

SAS Tips and Tricks in Clinical Programming - A Must-Read for Programmers in the Industry In clinical trials, efficiency and precision are key. Our talented Statistical Programming team at Quanticate have put together an overview guide of practical SAS tips and tricks to help clinical programmers streamline their work and avoid common pitfalls. From data manipulation to debugging, these insights can make a real difference in day-to-day operations. Take a moment to read the article below and share it with your network. Whether you’re new to clinical programming or a seasoned professional, there’s always something to learn. https://hubs.li/Q02Wql310 #ClinicalProgramming #SAS #ClinicalTrials #DataScience #CRO

Collaborating to Rescue Challenged Clinical Trials 🕐🌟 Clinical trials don’t always go as planned, and when obstacles arise, the value of collaboration becomes clear. At Quanticate, our approach to rescue studies is built on close partnerships with our clients. By working together, we can swiftly diagnose the issues at hand and offer tailored solutions that restore a trial's integrity. Rescuing a study isn’t just about data recovery, it’s about understanding the bigger picture, maintaining patient safety, and ensuring the study can proceed with renewed purpose. At Quanticate we take great pride in consistently delivering thoughtful, data-driven strategies in the most complex situations. It’s through these collaborations that we truly make a difference 👥 To find out more about our rescue study services, click below 👇 https://hubs.li/Q02Vg8Px0 #RescueStudies #Collaboration #CRO #ClinicalTrials #Partnerships #Quanticate #ClinicalResearch

Preparing Integrated Summaries of Safety (ISS) and Efficacy (ISE) for regulatory submissions can be complex, with each submission bringing its own unique challenges. Our guide simplifies this process by outlining key strategies to help you plan and execute your ISS/ISE efficiently. Download our free whitepaper to learn how to: 📝 Plan analyses and summaries 📊 Manage data submissions and timelines 🔧 Minimize workloads and reduce production issues Click this link to download now: https://hubs.li/Q02V37Yh0 #RegulatoryCompliance #IntegratedSummaries #ClinicalTrials #RegulatorySubmission #Whitepaper

✨Are you seeking additional resources as quickly as possible? ✨ Whether you're looking for a biometric functional service provider (FSP) or support for a particular therapeutic area, gain rapid access to our experienced teams and become flexible to any peaks and troughs in your pipeline with high-quality clinical data solutions. To find out more about our scalable FSP solutions, click below to request a consultation👇 https://hubs.li/Q02SVj1g0 #Quanticate #BioTech #FunctionalServices #BiotechExperts #ClinicalTrials #DataScience

Inside Project Optimus - FDA’s Initiative to Optimise Oncology Treatments The FDA's #ProjectOptimus aims to modernise oncology treatment by refining dose selection methods, shifting from a "maximum tolerated dose" approach to one that balances efficacy with long-term safety. This initiative could greatly improve cancer treatment by optimising drug doses for both effectiveness and patient quality of life. Our recent article explores these important changes in oncology clinical trials and highlights the challenges and strategies involved. To learn more about how Project Optimus is reshaping cancer treatment development, read our full article here: https://hubs.li/Q02SvXDn0 #Oncology #ClinicalTrials #CancerResearch #FDA #Pharmaceuticals #DrugDevelopment #OncologyInnovation #PatientSafety #PrecisionMedicine #Quanticate

NEW 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 our latest 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/Q02RCj7r0 #Pandemic #VaccineDevelopment #PharmaInnovation #BiotechSolutions #ClinicalDataExperts #ClinicalProgramming #RapidResponse #BigPharma

Achieving true efficiency in clinical programming requires a balanced perspective over a narrow perspective. In our free whitepaper, our experts explore the balanced approach to program and data efficiency, showing how each 'micro efficiency' contributes to the bigger picture. Discover: ⚖️ The distinction between micro and overall program efficiencies. 🔍 How narrow perspectives can lead to inefficiency. 🚀 Real life examples of balancing speed and innovation costs for long-term success. See how a balanced perspective can make a real difference in your clinical trials. Download our whitepaper now: https://hubs.li/Q02RbLYn0 #ClinicalTrials #Programming #DataEfficiency #Biometrics #ClinicalResearch #ClinicalProgramming #DataScience

📢 Unlock the Secrets to SAS Macro Success in Clinical Trial Reporting In our free whitepaper, we cover everything you need to know about SAS Macros, addressing common pitfalls, as well as highlighting the key elements of a successful process improvement project, such as the production of macros that simplify table creation with a single call. Discover valuable insights on: ✅ Planning Your Process Improvement Project ✅ Setting Realistic Expectations ✅ Harnessing the Power of Utility Macros ✅ Maximising Macro Flexibility ✅ Enhancing User-Friendliness ✅ Ensuring Adoption of New Macros ✅ Reaping the Benefits of Innovative SAS Macros Ready to elevate your SAS skills and bring efficiencies to your trial reporting? Download our free whitepaper today. 🔗 https://hubs.li/Q02QKCdz0 #SASMacros #ProcessImprovement #DataExpertise #SASprogramming

Rare disease clinical trials pose unique challenges, from small patient populations and slow recruitment to lack of controls due to ethical reasons and choice of suitable endpoints. At Quanticate, we’ve spent over 30 years helping Sponsors overcome these issues with our tailored solutions. Recently, we supported an orphan drug study on recombinant human C1 inhibitor for hereditary angioedema, providing both statistical and medical writing expertise. We’ve also worked on prevalence estimates for orphan drug applications in Parkinson’s disease and head and neck cancers. Our specialist biometric services help you master the complexities with smart data management, robust statistical analysis, and trial designs that work with small sample sizes. Learn how our rare disease expertise can help your trials succeed - https://hubs.li/Q02PwTXC0