CT Image of Pulmonary VeinsAtrial fibrillation remains a leading cause of death and disability and the most common type of arrhythmia. While radiofrequency ablation and cryoablation are two established methods of treatment, in recent years more research has been...
Harnessing AI Technology to Identify Adverse Events with Great Accuracy and Efficiency
The use of technology in clinical trials, including artificial intelligence (AI), is evolving rapidly. According to the consulting firm Gartner, “The life science industry stands at an inflection point driven by emerging technologies spanning AI, automation, and...
The Power of Generative Artificial Intelligence in Medical Writing
The use of artificial intelligence (AI) in clinical trials is evolving quickly. According to the research and consulting firm, Gartner, the life sciences industry is experiencing a “boom” in AI-powered drug development. AI technology is already being applied to early...
Five Advantages of Veranex’s Quality Management Systems
Our approach to Quality Management ensures that we’re always speaking the same language. When it comes to needing a Quality Management Solution, there are numerous benefits to working with a CDMO like Veranex. We have the flexibility to adapt to the client’s needs...
Built to Fit Your Needs: Our CDMO Capabilities
Learn about our capabilities and offerings as a CDMO We sat down with Bill Croisetiere (VP, Integrated Supply Chain), Chris Vigneau (VP, Manufacturing Solutions) to discuss our unique approach to manufacturing as a CDMO. Being both horizontally and vertically...
Does Size Matter? Rescue from a large CRO
THE CHALLENGE Missed timelines and EDC build errors compromised the potential success of the company’s phase 1 study.THE SOLUTION Experienced team members and robust internal reviews resulted in a timely, high-quality EDC build and data management plan.THE OUTCOME...
Prioritizing Patient Safety and Fostering Innovation with the MHRAs New Roadmap for Medical Devices
On January 9, the United Kingdom (UK)’s Medicines and Healthcare Products Regulatory Agency (MHRA) released a regulatory framework - Roadmap towards the future regulatory framework for medical devices. The comprehensive plan charts the course for strong regulations...
Strategies for Successful Clinical Data Management Rescue Studies
What is a rescue study? A rescue study is a clinical trial that is being conducted by a new vendor after having previously been conducted by another vendor or in house by the sponsor. The reasons for the change may be based on issues negatively affecting timelines,...
Artificial Intelligence (AI), General Data Protection Regulation (GDPR) and Cybersecurity: 10 Misconceptions About Medical Device Software
Medical Device Software (MDSW) is a growing, fast-evolving industry. However, manufacturers must often face a regulatory framework which does not evolve at the same speed. Regulation for medical devices is restrictive, since it needs to guarantee the safety...