Case Study: One of the largest and longest running CROs in Australia selects Cloudbyz eClinical Platform to drive growth
Customer Overview
Established in 1993, the customer is one of Australia's largest and most experienced clinical trial establishments. Their team specializes in a range of early-phase clinical trials...
Case Study: Leading CRO in New Zealand partners with Cloudbyz to improve its’ clinical operations
Customer Overview
The company was formed in 2020 by the merger of 2 reputed clinical research establishments in New Zealand, and is the country's leading early phase clinical research provider. The...
Point of View: The Future of Clinical Trials with Salesforce's Agentforce and Cloudbyz eClinical
Salesforce's newly launched Agentforce platform, a powerful AI-driven solution, is set to transform various industries, including life sciences and clinical trials. Agentforce’s AI-powered agents go...
Quality by Design (QbD) in Clinical Trials: A Metrics-Driven Approach to Enhancing Quality
The Clinical Trials Transformation Initiative (CTTI) advocates for improving clinical trial quality and efficiency, with a focus on patient safety and reliable outcomes. Quality by Design (QbD)...
MHRA GPvP Inspection Programme: Latest Guidelines and Insights from 2024 Inspections
The MHRA's Good Pharmacovigilance Practices (GPvP) Inspection Programme is a critical regulatory mechanism designed to ensure that Marketing Authorisation Holders (MAHs) meet pharmacovigilance...
Comprehensive Guide to Edit Checks in eCRFs for Clinical Trials: Ensuring Data Integrity and Regulatory Compliance
In clinical trials, ensuring data quality is crucial for both the success of the trial and regulatory compliance. Electronic Case Report Forms (eCRFs) have become an essential tool for capturing...
Supporting Each Step of the Clinical Trials Toolkit with Cloudbyz eClinical Solutions
Clinical trials are complex endeavors, requiring the meticulous coordination of numerous stages, regulatory frameworks, and ongoing management. From planning to post-trial activities, ensuring...
Transforming IDE Studies: The Impact of EDC and Safety Solutions on Efficiency and Compliance
In today’s fast-paced medical device industry, ensuring patient safety and meeting regulatory compliance is more crucial than ever. The rise of advanced technology has brought about...
Scaling Biopharma R&D: A Strategic Vision for the Future
Biopharma remains one of the most important contributors to global health innovation. However, the changing scenario with rising R&D costs, increasingly complex regulatory landscapes, and...
Cloudbyz EDC: Recognized as a Major Contender in the 2024 Everest Group Report
The global life sciences landscape is rapidly evolving, and with that, the demand for innovative solutions to streamline clinical research and data management has never been more pressing. In this...
Case Study: One of the largest and oldest cancer research institutes in the US partners with Cloudbyz to undertake transformation of its eClinical landscape
Customer Overview
Founded in 1923, the institute is at the forefront of radiology evolution, representing more than 41,000 diagnostic and interventional radiologists, radiation oncologists, nuclear...
Case Study: Leading UAE based CRO transforms digitizes clinical research with Cloudbyz eClinical
Customer Overview
The customer, a leading health-tech company, is on a mission to develop a world-class healthcare sector in the UAE and beyond. It is the first UAE-based CRO specializing in...
Case Study: Leading CRO partners with Cloudbyz to optimize end-to-end clinical trial operations
Customer Overview
The customer is a leading CRO running clinical trials in community oncology sites in the US. Focused on community-based Hematology & Oncology research sites, they provide...
Case Study: US based CRO partners with Cloudbyz to move their clinical trial operations to cloud
Customer Overview
The customer is a trial management organization connecting IVD manufacturers and pharmaceutical companies with a network of doctors participating in advancing medical research. It...
Case Study: Global Pharma company selects Cloudbyz’s clinical research platform to run clinical trials
Customer Overview
The customer is a leading multinational pharmaceutical company based in India and overseas, and is committed to providing affordable and innovative medicine for healthier lives....
Maximizing Early-Stage Trials with Cloudbyz EDC: Unleashing the Power of Data and Technology in Phase 1 Clinical Trials
Introduction
Early-stage clinical trials, particularly Phase 1 trials, are critical for determining the safety, tolerability, and pharmacokinetics (PK) of new drugs. These trials lay the foundation...
Ensuring Data Security and Compliance in Clinical Trial Management Systems (CTMS)
In the rapidly evolving landscape of clinical research, data has become one of the most valuable assets. Clinical Trial Management Systems (CTMS) play a pivotal role in managing this data,...
CTMS Implementation Best Practices: Ensuring a Successful Transition to a Robust Clinical Trial Management System
Implementing a Clinical Trial Management System (CTMS) is a critical step for any life sciences organization aiming to enhance the efficiency, compliance, and oversight of their clinical trials....
Pharmacovigilance Software Solutions for CROs: What to Consider
Contract Research Organizations (CROs) play a vital role in the life sciences industry, acting as the bridge between pharmaceutical companies and regulatory bodies. They are tasked with managing...
How CTMS Enhances Clinical Trial Efficiency and Compliance
Clinical trials are the backbone of medical advancements, but their complexity and the regulatory environment pose significant challenges to researchers, sponsors, and clinical trial managers. The...
The Impact of Real-Time Analytics in Clinical Trial Management
In the fast-paced and data-driven world of clinical trials, the ability to access, analyze, and act on data in real time is becoming increasingly critical. Real-time analytics is transforming how...
Emphasizing Process-Level Unification and Real-Time Collaboration in Clinical Trial Management
In the complex and highly regulated world of clinical trials, the ability to efficiently manage and integrate multiple processes is critical. Life sciences companies often face challenges related to...
Clinical Research during Recession: How Unified eClinical solutions are helpful?
Economic recessions cut across many industries; the clinical trials sector is no different. As with most other sectors, the recession puts pressure on the clinical trials to remain innovative yet...
Conducting Sustainable Clinical Trials- A step in the right direction
With the problems of climate change continuing to grow, the footprint of the pharmaceutical industry on the environment is under pressure for reduction. Clinical trials, as a major portion of...
Skipping Informed Consent for In Vitro Diagnostic (IVD) Trials: Understanding the Exceptions
Understanding the exceptions in Informed consent is an essential aspect of ethical clinical research because it concerns full awareness of risks and benefits related to research, as well...
FDA’s Accelerated Approval Program: Empowering Timely Access to Critical Treatments and the role of eClinical
The Accelerated Approval Programof the FDA provides for conditional approval of drugs that show an effect sufficiently desirable, compared to available medications, based on surrogate endpoints...
The impact of eClinical platforms in enabling Patient-Centric research
In the ever-changing landscape of clinical research, patient-centricity has become a pivotal focus. Traditional methods often overlook the needs and experiences of patients, leading to lower...
Indicators Your Clinical Trial is Not Patient-Centric
In recent years, the shift towards patient-centric clinical trials has become paramount. A patient-centric approach not only ensures higher patient satisfaction but also improves recruitment,...
Addressing Social Determinants of Health in Clinical Trials and Role of eClinical Systems
Social determinants of health (SDOH) encompass non-medical factors that significantly influence health outcomes. These factors include socioeconomic status, education, neighborhood and physical...
Understanding FDA’s Draft Guidance on Cancer Clinical Trial Eligibility Criteria: Performance Status
TheFDA’s draft guidancemarks a significant step toward more inclusive and relevant cancer clinical trials. Aimed at industry stakeholders, IRBs, and clinical investigators, this document...
Improving Inclusion in Clinical Trials: FDA's Draft Guidance on the Use of Laboratory Values
The draft guidance by the FDA represents a significant step toward making clinical trials more inclusive and representative of real-world populations. This guidance aims to correct overly...
Buyer’s Checklist for selecting the right CTMS vendor
Selecting the right Clinical Trial Management System (CTMS) is crucial for the success of your clinical trials. A robust CTMS not only streamlines trial management but also ensures regulatory...
Buyer’s Checklist for Selecting the Right eTMF Vendor
Choosing the right Electronic Trial Master File (eTMF) system for your clinical trials is vital. It ensures efficient document management, smooth submissions to regulatory bodies, and keeps your...
Breaking Down Financial Barriers in Clinical Trials: Enhancing Equity and Access for Patients
Despite the critical role that clinical trials play in advancing medical progress, there's a significant issue that often goes unnoticed: the lack of diversity among participants. This disparity...
How the New EU AI Act Will Impact Clinical Trials in the Life Sciences?
The European Parliament recently passed the EU’s newAI Act, which is now awaiting final approval. This Act is poised to significantly change the clinical trials landscape within the life sciences...
Buyer Checklist for Security Assessment of eClinical Vendors
Clinical trials are the backbone of medical research, driving innovation and ensuring the safety and efficacy of new treatments. With the rise of eClinical systems, the management of clinical trials...
Buyer’s Checklist For Selecting The Right eSource Vendor
Selecting the right eSource system for clinical trials is a critical decision that can significantly impact the efficiency and success of your research projects. An eSource system not only...
Learn how the Cloudbyz Vet eClinical Platform aligns with the latest FDA guidelines
The FDA Center for Veterinary Medicine (CVM)’sdraft guidanceon pharmaceutical development for veterinary medicines outlines a systematic approach to ensure the quality, safety, and efficacy of...
Buyer’s Checklist for selecting the right EDC vendor
Selecting the right Electronic Data Capture (EDC) system is vital for the success of clinical trials. An effective EDC system streamlines operations, ensures data quality, and enhances regulatory...
A closer look at Oncology Trials and the role of eClinical companies
In the high-stakes world of oncology, innovation races forward at breakneck speed, creating a dynamic environment where only the most agile and informed players can thrive. McKinsey & Company’s...
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...
Optimizing Clinical Trials with Unified Trial Management: Streamlining Processes and Ensuring Future Success
A Comprehensive Look at the Modernization of Clinical Trials through Unified Trial Management
Introduction:
Clinical trials are essential for the advancement of medicine and healthcare. As...
7 Benefits of integrating EDC with CTMS, eTMF and Safety
Integrating electronic data capture (EDC) with other clinical trial management systems like clinical trial management systems (CTMS), electronic trial master files (eTMF), and safety systems can...
