We know that diversity in our companies and communities brings a wealth of varied experiences and points of view. Did you know that diversity is also essential in clinical trials? One goal of a clinical trial is to represent the whole population within a disease state. Effectiveness, side effects and even performance of a device […]
The DZS Dispatch: June 2022
The DZS Podcast is LIVE! Check out our newest podcast episodes! Read the entire June Newsletter Other Articles ICH E6(R3) Revisions: Is Your Team Ready for the Coming Changes?
ICH E6(R3) Revisions: Is Your Team Ready for the Coming Changes?
ICH E6(R3) Revisions: Is Your Team Ready for the Coming Changes? With potential changes in the design and development process on the horizon, we discuss the upcoming ICH E6(R3) revisions and the impact on clinical research A Look Back at Revision Two In 2016, ICH E6(R2) was introduced, focusing on trial participant protections and […]
The DZS Dispatch: April 2022
Staying Vigilant with Pharmacovigilance -Click image to read full newsletter-
Staying Vigilant with Pharmacovigilance
What is Pharmacovigilance? Medicinal products have transformed how we treat and prevent diseases, but they may also have unexpected side effects. As defined by the World Health Organization, Pharmacovigilance is the science and activity relating to the detection, assessment, and prevention of adverse effects or any other drug-related problem. It is a key way to […]
Site Monitoring in the Time of COVID
Remote monitoring in the spotlight By Maria Paluselli, MS, Project Manager and Medical Writer, DZS Clinical Services The COVID-19 pandemic has impacted nearly every facet of daily life, including conducting clinical research trials. Quarantines, site closures, travel limitations, supply chain for investigational product and necessary equipment, and the possibility of staff or study patients becoming […]
Webinar: How CROs and Sponsors Improve TMF Management with a Shared eTMF
How CROs and Sponsors Improve TMF Management with a Shared eTMF For biotech, pharma and medical device sponsors considering TMF Management as an area where greater efficiency and transparency would be beneficial for your studies, DZS Clinical Services and Agatha partner in welcoming you to watch our recent webinar. The Trial Master File (TMF) is […]
The DZS Dispatch: February 2022
Best Management Practices for eTMF -Click image to read full newsletter-
Whitepaper | Beyond Storage: How CRO’s and Sponsors Work Together to Manage the Complexities of eTMF Oversight
The DZS Dispatch: December 2021
Challenges and Opportunities in Clinical Data Management Identifying and managing critical data points in clinical research is more important than ever. Forbes magazine recently reported that “Two-and-a-half quintillion bytes of data is collected daily.” Unprecedented amounts of information or “data points” are being gathered in almost every aspect of your personal and professional life, and […]