“By streamlining the process and providing the most advanced technology, we can provide yet another solution for simplifying the integration of electronic data capture (EDC) into clinical studies.
San Diego, CA (PRWEB) April 25, 2017
L3 Clinical Trials, the Clinical Research Organization (CRO) division of L3 Healthcare, is pleased to announce the company is now a certified iMedNet eClinical and Electronic Data Capture software designer for clinical trial data management. The iMedNet software certification enables the company’s clinical research team to build, customize and manage clinical trial data capture and databases for clients. In completing this certification, L3 Clinical Trials, continues to provide an integrated and comprehensive suite of services that can support an entire clinical trial program: from study concept to data analysis, reporting, and site level payments.
“A fully integrated clinical research organization that has the expertise, know-how and streamlined approach helps customers conduct clinical trials efficiently and cost-effectively,” said Chermaen Lindberg, Partner at L3 Healthcare. “Our certification allows us to manage all aspects of a clinical trial, obviating the need to utilize additional data management resources, apply add-ons, or subcontract with 3rd party data management vendors.” By eliminating these common but unnecessary complexities, L3 Clinical Trials is uniquely positioned to provide clients with premium services at the most affordable industry rates.
The L3 Clinical Trials’ business model is based on providing start-ups and mid-size in vitro diagnostic (IVD) and medical device companies with highly experienced resources that intuitively and effectively function as part of their clients’ project teams. In obtaining the certification through iMedNet, L3 Clinical Trials reinforces its integrated and collaborative approach with consistent staff resources throughout the process, fostering the best possible environment and identifying cost-effective clinical trial solutions.
“We pursued iMedNet certification so that we can deliver several unique and time-saving steps for our sites and our sponsors, such as the ability to access and use the system on multiple platforms and provide electronic-entry adjudication capability,” said Jane Edwards, VP Clinical Research at L3 Healthcare. “By streamlining the process and providing the most advanced technology, we can provide yet another solution for simplifying the integration of electronic data capture (EDC) into clinical studies. This improves workflow for clinicians and research coordinators while helping contain costs.”
About L3 Healthcare
L3 Healthcare, founded by IVD and medical device professionals, provides proven pre- and post-market expertise and resources dedicated to assisting organizations with generating clinical evidence, establishing clinical value and increasing market adoption in the global marketplace. L3 Clinical Trials, a division of L3 Healthcare, focuses its services on devising and executing clinical trials through streamlined processes, staff, technology and its vast key opinion leader and research network in the biotech and life science industries. The L3 Clinical Trials team understands the importance of strategically approaching clinical trials and go-to-market projects in environments with limited funds and resources, and seamlessly fills in the gaps where needed to achieve the desired goals. L3 specializes in key disease states and global markets that help provide value and a distinct edge for its clients. For more information, visit http://www.L3clinicaltrials.com.
About iMedNet
MedNet Solutions is a leading healthcare technology company specializing in electronic data solutions designed for the global life sciences community. MedNet’s proven, flexible and easy-to-use cloud-based eClinical systems dramatically improve the efficiency of clinical studies and registries of all types and sizes. Beyond simply electronic data capture (EDC), MedNet’s solutions deliver the tools and dashboards required to expertly manage all aspects of clinical research. Since 2001, pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted MedNet to consistently deliver the technology innovation, experience and reliability they need for success. For more information, please visit http://www.mednetsolutions.com/