We are pleased to announce that this year we will be joining PHUSE EU Connect 2021 as delegates and sponsors of the hands-on workshop “Clinical Trial Safety Analyses – Common Pitfalls and FAQ” conducted by Eli Lilly. Event information: Event format: Hybrid Date: 15 – 19 November 2021 Registration & agenda: available on the official website…
This year we had the pleasure of joining the Clinical Trials Europe 2021 as speaker and sponsor. Katell Bernois, our Director of Statistical Consulting, and Paula Yates, Senior Director, Biostatistics & Data Management, delivered a presentation titled “7 Steps to Maximise the Effectiveness of Your CRO Partnership”. Abstract of the “7 Steps to Maximise the Effectiveness of…
Integrating data for submissions can be a laborious and difficult task. Even with CDISC data, it can be a mammoth undertaking but when we add legacy data in the mix then it can make things far more difficult. One of the ways of ensuring your approach to integration is effective is to have a good…
While the Sponsor/CRO relationship is common, its effectiveness can be reduced due to miscommunication about expectations and inadequately defined responsibilities and accountabilities. By developing key strategies and documents, you can significantly boost the effectiveness of your CRO partnership, allowing you to leverage the collaboration to meet critical clinical trial benchmarks and milestones, on time and…
This year, we had the pleasure of joining Outsourcing in Clinical Trials Europe as sponsors and as speakers. Event information: Event format: Virtual Date: 5th-6th May, 2021 At Outsourcing in Clinical Trials Europe, Amanda Cross, our Executive Director of Service Strategies, presented a speech titled “Defining a Data Strategy: How to effectively manage your key asset”. Speech…
On the 3rd of December, we conducted a new webinar titled “Leveraging Digital Transformation: How to Approach Decentralised Trials” – during this webinar, the participants were able to interact with the speakers and left up to speed with the latest technologies and approaches, and with practical advice on planning and executing their own decentralised trial…
On the 17th of November, we conducted a new webinar titled “Effective Trial Design: Clinical Trials in Small Patient Populations”. Designing and conducting clinical trials in indications with inherently small patient populations, such as rare disease, can be quite difficult. The limited number of patients available for the trials has a direct impact on the…
On the 21st of July 2020 CROS NT conducted a webinar focused on clinical trial data oversight. During the webinar titled “Clinical Trial Data Oversight: Why and How?”, we reviewed oversight as it relates to data collection and reporting, analysed options for oversight including an assessment of different approaches, discussed the benefits of a centralized…
On the 28th of May 2020 CROS NT conducted a webinar focused on current trial designs that can help to decrease the risk of failure and reduce the costs, we have also discussed their advantages and disadvantages. Webinar learning outcomes: Basics of adaptive designs How to evaluate the benefit of an adaptive design for biopharma…
On the 31st of March 2020 CROS NT conducted a webinar focused on the ways statistical programmers can work in dual roles and expand their skill set, as well as support different operational groups and get involved in the upfront project planning. Webinar learning outcomes: Importance of retaining employees through professional development How statistical programmers…
On the 9th of April 2020 CROS NT conducted a webinar focused on the use of enrichment designs for reducing placebo response and thereby enhancing signal detection. This webinar described the use of a Sequential Parallel Comparison Design (SPCD) to increase the chance of success of clinical trials, especially trials with possibly high placebo effect.…