Smart Budgeting = Successful Trials! Clinical trials demand precise budgeting to avoid delays, overruns, and compliance risks. ?? Fair Market Value (FMV) ensures transparent compensation ?? Real-time budget tracking prevents financial surprises ?? Automated budgeting tools improve efficiency Are you using the right strategies to keep your trial on track? Let’s chat below! ?? ?? Read more: https://hubs.ly/Q037hvGR0 #ClinicalTrialFinance #BudgetOptimization #LifeSciences
Cloudbyz
软件开发
Naperville,Illinois 9,249 位关注者
One Platform. Endless Possibilities. CTMS, CTBM, eTMF, EDC, ePRO & eCOA, PR and Safety & Pharmacovigilance.
关于我们
Cloudbyz is focused on building cloud-based products and solutions for life sciences customers, and help them innovate drug development and research to bring therapies faster to market which improve patient health and saves lives. Our innovative digital solutions for Pharmaceuticals, Contract Research Organizations (CRO) and Medical Devices companies helps to digitize research, drug and device development and commercialization. Our suite of products include: 1. Cloudbyz CTMS 2. Cloudbyz CTBM 3. Cloudbyz eTMF 4. Cloudbyz EDC, ePRO & eCOA 5. Patient Recruitment 6. Cloudbyz Safety & PV 7. ClinicalWave.ai (AI based platform for Life sciences organizations) Cloudbyz CTMS, eTMF, EDC, and Safety & Pharmacovigilance are built 100% native on Salesforce cloud platform for sponsors, clinical research organizations (CRO), and Clinical Sites. Cloudbyz Clinical Research Solutions are flexible and scalable to enable to manage and collaboration on clinical trial operations while the intuitive, straightforward design allows rapid deployment with a very intuitive and easy-to-use cloud-based solution. Cloudbyz ITPM offers 360° view and real-time visibility across IT planning, execution, and operations and helps organizations to achieve agility, velocity, innovation, and collaboration across IT and business. Cloudbyz ITPM helps CIO, PMO, and IT leaders to visualize the IT landscape, capability mapping, investment, and operational health in real-time and better align IT initiatives with business.
- 网站
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https://www.cloudbyz.com
Cloudbyz的外部链接
- 所属行业
- 软件开发
- 规模
- 51-200 人
- 总部
- Naperville,Illinois
- 类型
- 私人持股
- 创立
- 2014
- 领域
- Clinical Trial Management、eTMF、eConsent、PPM、Project Portfolio Management、eCRF、ePRO、eCOA、RBM、Study Start Up、VirtualTrials、Clinical Research、CRO、RTSM、EDC、Pharmacovigilance、Drug & Device Safety、Signal Management、CTMS、AI、Data Redaction、Data Extraction、DICOM Image Processing和DICOM Data Redaction
地点
Cloudbyz员工
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Tom Hedgecoth
Leading Highly Productive Teams through Business Transformation?? Strategist & Technologist ?? 2023-Completed 100% of Trailhead Badges in 8 months ??…
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Dinesh Kashyap
Next-Gen Unified eClinical on Salesforce | AI | CTMS | CTFM | eTMF | EDC | eCOA | ePRO | RTSM | Safety & PV | RWE | Patient Recruitment
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Hariharan Ramadoss
Co-Founder - Cloudbyz Inc.
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Sugandha Anand
Associate Director- Human Resources
动态
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Clinical Teams, Let’s Talk Site Visits & Compliance! Managing site visits & compliance shouldn’t feel like a constant uphill battle. Yet, many clinical teams still face: ? Inefficient site monitoring workflows ? Compliance risks & last-minute audit stress ? Lack of real-time oversight What if there was a better way? Join us for a LIVE webinar where we’ll break down proven strategies to optimize site visits, streamline compliance, and enhance oversight using Cloudbyz CTMS. What you’ll gain from this session: ? Best practices to make site visits more efficient ? How to stay audit-ready without extra admin burden ? A practical look at how Cloudbyz CTMS improves oversight ?? March 27, 2025, 11 AM EST ?? Live Webinar ?? Secure your spot! https://lnkd.in/gFihUxpN Who should attend? If you’re in Clinical Operations, Trial Management, or Compliance, this session is for you! Tag your colleagues who should be part of this conversation! Let’s discuss how to improve clinical trial oversight together. #ClinicalTrials #SiteVisits #Compliance #CTMS #ClinicalResearch #ClinicalOperations #Webinar
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How efficient are your site visits? Site monitoring is a critical component of every trial, yet clinical teams often face: ? Compliance gaps ? Manual, time-consuming workflows ? Inefficient oversight Join us for a live webinar to learn how to streamline site visits, enhance compliance, and improve oversight efficiency with Cloudbyz CTMS. What You’ll Learn: ? Best practices for site visit & compliance management ? Strategies to stay audit-ready without extra admin burden ? How Cloudbyz CTMS enhances real-time oversight ?? March 27, 2025, 11 AM EST ?? Register now! → https://bit.ly/3XueHyW Let’s redefine how clinical teams handle site visits. #CTMS #ClinicalTrials #Compliance #ClinicalResearch #SiteVisits
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Great software is simple, scalable, and high-quality. Yet, many teams struggle with overcomplicated processes that slow innovation. The solution? ?? Keep quality simple with: ?? Agile development for flexibility ?? Automated testing for efficiency ?? User-focused design for clarity Are you making quality a priority without adding complexity? Let’s discuss below! ?? ?? Read more: https://hubs.ly/Q037hvyx0 #SoftwareDevelopment #QA #KeepItSimple
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Data is the backbone of clinical research—so why risk losing it? ?? Best practices for clinical trial data archiving: ? Implement secure, compliant storage solutions ? Use cloud-based & AI-driven data management tools ? Maintain audit trails & version control for integrity Is your data archiving regulatory-ready? Let’s discuss below! ?? ?? Read more: https://hubs.ly/Q037hvKF0 #ClinicalTrialData #EDC #HealthcareInnovation
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21 CFR Part 11: A Must-Know for Digital Clinical Trials If your clinical trial relies on electronic records and signatures, compliance with 21 CFR Part 11 isn’t optional—it’s essential. ?? What’s required? ?? Secure system access & authentication ?? Tamper-proof audit trails ?? Validated e-signatures that meet FDA standards Non-compliance can lead to costly delays & regulatory risks. Is your system audit-ready? Let’s discuss below! ?? ?? Learn more: https://hubs.li/Q037hvB00 #ClinicalTrials #Compliance #DigitalHealth
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The Future of Medical Devices is Digital! ?? Traditional → Digital transformation is reshaping healthcare: ?? AI & Big Data for predictive diagnostics ?? Wearable tech for real-time health tracking ?? Telemedicine & remote care improving patient access ?? Cybersecurity to protect sensitive health data The future is clear: Smart, connected, patient-centric devices are here to stay. ?? What’s the biggest digital breakthrough you’ve seen in MedTech? Let’s discuss below! ?? ?? Read more: https://hubs.li/Q037hvGD0 #DigitalHealth #MedicalTechnology #HealthcareInnovation
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Clinical trials depend on precision—from randomizing patients to ensuring sites receive the right supplies at the right time. But manual processes and outdated systems can lead to delays, errors, and compliance risks. With Cloudbyz Randomization & Trial Supply Management (RTSM), sponsors and CROs can streamline patient randomization and optimize trial supply logistics—all in one cloud-based solution. ? Flexible randomization methods – Block, stratified, adaptive, and more ?? End-to-end supply management – Reduce waste & prevent stockouts ?? Real-time tracking & forecasting – Improve decision-making with AI-driven insights ?? Regulatory-compliant & audit-ready – Meet FDA, EMA, and ICH GCP standards By automating RTSM, trials become more efficient, cost-effective, and compliant—helping life-saving treatments reach patients faster. ?? Ready to streamline randomization & trial supply? Learn more ?? https://hubs.li/Q035VW_S0 #RTSM #ClinicalTrials #LifeSciences #Cloudbyz #ClinicalResearch #TrialManagement
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Imagine this: A groundbreaking drug trial is delayed by six months because of inconsistent data entry across trial sites. The ripple effect? Increased costs, compliance risks, and delayed patient access to life-saving treatments. This isn’t just hypothetical—it’s a reality for many research teams. The good news? Robust data management practices can help prevent these costly delays. In your experience, what’s the biggest data management challenge in clinical trials? Vote below! ?? ?? Data inconsistency ?? Slow reporting & analysis ?? Compliance & regulatory hurdles ?? Other (Comment below!) #ClinicalTrials #LifeSciences #DataIntegrity ?? Learn more: https://hubs.li/Q037hvrW0