Pharmacovigilance Made Easy with Salesforce-Based Platform
Discover how a pharmacovigilance solution built on the Salesforce platform can streamline adverse event reporting, enhance patient safety, and improve compliance.
February 27, 2023
Dinesh Kashyap
CEO
Dinesh is a distinguished visionary leader with more than 20 years of experience in the IT industry. He has an impressive track record in strategy and management consulting, business & IT transformation, innovative digital platform implementations, building practice and capabilities in new niche markets. Prior to founding Cloudbyz, Dinesh was with HCL where he led a multi-million dollar business. You can find Dinesh on LinkedIn.
Saving Time and Improving Quality: Medical Coding Automation in Pharmacovigilance
pharmacovigilance medical coding automation is a promising and rapidly evolving field that has the potential to revolutionize the way pharmacovigilance professionals monitor and assess medication safety. By leveraging the power of AI and machine learning, pharmacovigilance organizations can streamline the medical coding process, improve the accuracy and consistency of ADR reporting, and gain new insights into medication safety trends and risks.
February 25, 2023
Transforming Clinical Study Build with Generative AI: Automating Data Extraction from Protocol Documents in Cloudbyz EDC
Generative AI has the potential to revolutionize the clinical study build process by automating data extraction from protocol documents. With its ability to process natural language and understand contextual nuances, it offers unparalleled speed, accuracy, and efficiency. Cloudbyz EDC, when integrated with generative AI, can enable researchers and organizations to accelerate their clinical trials, reduce costs, and improve data quality. As the field of clinical research continues to advance, embracing generative AI will be key to staying competitive and compliant in an increasingly complex regulatory landscape.
September 19, 2023
A Deep Dive into Best Practices for Clinical Trial Site Start-Up
Setting the initial stages right in a clinical trial is akin to laying the foundation for a building. The site start-up phase is that critical period where you’re not just laying bricks but ensuring they’re placed right. A stumble here can have a cascading effect on the entire trial. Let’s delve deeper into each of the best practices for an effective site start-up.
August 11, 2023
Why a Platform Approach is Vital for Clinical Research Management Transformation
The clinical research landscape is rapidly evolving. As it becomes
August 9, 2023
Discover the Power of Real World Evidence (RWE) on the Salesforce Platform
Unlock the potential of real-world evidence with our RWE solution on the Salesforce platform. Contact us today to discover how our solution can revolutionize your healthcare organization’s data-driven insights and drive superior patient outcomes.
July 12, 2023
Sensory Analysis and Consumer Research in New Product Development: Unveiling the Key to Success
Sensory analysis and consumer research are indispensable tools in new product development. By combining the scientific evaluation of sensory attributes with an understanding of consumer behavior and preferences, businesses can create products that satisfy and delight their target audience. Sensory analysis helps optimize product attributes, ensuring high-quality standards and consistency, while consumer research uncovers valuable insights to guide
June 21, 2023
Clinical Trial Data Archiving: Ensuring Efficiency, Compliance, and Accessibility
Clinical trial data archiving plays a vital role in maintaining data integrity, ensuring compliance with regulatory requirements, and fostering future research. By addressing challenges, following best practices, and leveraging digital solutions, organizations can establish efficient, secure, and accessible data archiving processes. Implementing robust archiving strategies not only protects valuable research data but also contributes to the overall advancement of medical knowledge and patient care.
June 16, 2023
Decentralized Clinical Trials: An In-depth Analysis
Decentralized clinical trials (DCTs) represent a significant evolution in the field of clinical research, harnessing the power of digital technology to enable more patient-centric, efficient, and inclusive trials. The shift from traditional site-based trials to decentralized models offers several advantages, including improved patient access and convenience, real-time data collection, reduced costs, faster recruitment, and enhanced diversity of trial participants.
June 11, 2023
Cloudbyz Pioneers Sustainability: Unleashing the Power of Regeneration
At Cloudbyz, we firmly believe that technology and nature can harmoniously coexist, leading the way to a sustainable future. Our sustainability initiative is a significant stride towards a world where digital transformation and ecological responsibility are intertwined, moving towards a future where the prosperity of our planet and its people is the ultimate measure of success.
Join us on this transformational journey as we pioneer a future where sustainability is not just an aspiration, but a reality.
June 9, 2023
Mastering Sensory Research: Techniques, Best Practices, and Future Directions
Sensory research is a powerful tool in the consumer goods industry. It provides invaluable insights into the complex interplay between products and human senses, driving the development of products that not only meet consumer needs but also provide enjoyable and memorable experiences. As technology continues to evolve, so too will the ways we apply sensory research, leading to even more exciting and innovative products in the future.
June 1, 2023
Navigating Digital Transformation in Clinical Trials: Essential Steps for eTMF Implementation
Implementing an eTMF system is a significant undertaking, but with careful planning and attention to detail, it can greatly benefit your organization. By following this eTMF implementation checklist, you can set your organization up for success, improving efficiency, compliance, and overall management of clinical trial documentation.
May 14, 2023
Streamlining Clinical Trials: The Impact of Unified Management Platforms on Drug Development
By implementing a unified digital platform, organizations can realize numerous benefits in terms of efficiency, cost savings, data quality, and overall effectiveness. These advantages contribute to a more streamlined and successful drug development process, ultimately helping organizations bring new treatments to market faster and at a lower cost.
May 4, 2023
Visibility of Payments for Sites: Enhancing Transparency and Streamlining the Process
Financial transparency and timely payments are essential for maintaining strong relationships with clinical sites and ensuring their continued participation in trials. As the landscape of clinical research evolves, it is crucial for sponsors and CROs to adopt innovative solutions and strategies that address the challenges associated with clinical site engagement, particularly regarding payment visibility.
May 4, 2023
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