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.

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.

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

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.

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.

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.

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.

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.

Preparing for the New EU-CTR: A Step-by-Step Guide and SOPs for Compliance

The new EU Clinical Trial Regulation replaces the previous Clinical Trials Directive and aims to improve patient safety and enhance transparency in clinical research. This article provides a step-by-step guide for preparing for the new Regulation, including understanding the changes, reviewing current clinical trial protocols, assessing the impact on your trial, developing new documents and procedures, training staff, preparing for centralized authorization, ensuring transparency, and staying up to date with new guidance. Additionally, the article suggests several Standard Operating Procedure (SOP) documents that could help adhere to the new Regulation, including Protocol Development SOP, Informed Consent SOP, Data Collection and Reporting SOP, Centralized Authorization SOP, End-of-Trial Reporting SOP, Training SOP, and Quality Control and Assurance SOP.

Join our email list to stay up to date on relevant and informative industry insights
Lead Source

At Cloudbyz, our mission is to empower our clients to achieve their business goals by delivering innovative, scalable, and intuitive cloud-based solutions that enable them to streamline their operations, maximize efficiency, and drive growth. We strive to be a trusted partner, dedicated to providing exceptional service, exceptional products, and unparalleled support, while fostering a culture of innovation, collaboration, and excellence in everything we do.

 

Subscribe to our newsletter

ISO 9001:2015 and ISO 27001:2013 Certified