Cmed presents at Mobile in Clinical Trials and Dpharm 2017
14 Aug 2017
Cmed has announced it will present its encapsia® clinical data suite at Mobile in Clinical Trials and DPharm: Disruptive Innovations to Advance Clinical Trials 2017. Attendees at both conferences will have the opportunity to learn about how encapsia® streamlines the capture, management and reporting of clinical data, helping trial sponsors to build more agile and flexible trial programs, while improving the accuracy of data and time-to-market for new drugs.
Mobile in Clinical Trials takes place on September 6, 2017 at the Marriott Copley Place, Boston.
Attendance at a recent event on Electronic Source Data (1) (eSource) confirmed that data held within Electronic Health Record and Electronic Medical Record (EHR / EMR) Systems are increasingly being used as the source for clinical trials. This practice imposes stringent requirements upon those EHR / EMR Systems; requirements that may not have been considered at the time of their original development, procurement and implementation.
Clinical research regulations require that all data collected as part of a clinical trial has a high degree of assured integrity.
In a previous article I have discussed Why eSource? The answer is clear. The demand for real time data in clinical trials continues to grow because of the need for faster access to safety signals, faster access to decision making data, such as patient eligibility and dose escalation, faster access to efficacy data. And what does this speed ultimately provide? Not only can the industry get lifesaving products to the patient sooner, money can be saved during the process.