New York, NY (PRWEB) May 14, 2012
Target Health Inc, is pleased to announce its implementation of the Verified Clinical Trials (VCT) clinical trials database registry in attempt to stop dual enrollment in clinical trials. Multiple simultaneous enrollments have become a serious problem in clinical research due to research volunteers who attempt to earn more money by jumping from one study to another without waiting for enough time to lapse between treatments. The professional clinical research volunteer not only creates additional liabilities for the drug manufacturer and the research site, but also places the health of the volunteer at risk and may compromise the integrity of clinical data. Target Health's commitment to clinical research volunteer safety and data quality has led them to implement the Verified Clinical Trials database registry system. This week Target Health launched the Verified Clinical Trials database registry system in their latest clinical Trial.
Dr. Jules Mitchel, President of Target Health Inc., stated, "Target Health has been an industry leader and improving outcomes and safety in clinical trials with innovative technology and expertise in regulatory affairs. We are pleased to partner with Verified Clinical Trials (VCT). Verified Clinical Trials provides added safety and quality to both early and late phase trials and offers so many other tools to the research site as well".
Dr Mitchel further added, "We are impressed with the ability of the Verified Clinical Trials system to easily and instantly have thousands of sites and users initiated without the need for software or hardware installation. VCT has assembled the perfect system to provide extended network coverage that will be required for a comprehensive North American clinical trials database registry."
Judith Schloss Markowitz, Senior Project Manager at Target Health, commented "The system is truly impressive. It has so many useful features for both the site and sponsor. VCT will improve safety and enhance study retention and reduce protocol deviations."
Dr. Mitchell Efros, President and CEO of Verified Clinical Trials, stated "We are thrilled to offer our services and clinical trial database registry to Target Health and be recognized by such a leading and innovative company." Efros further added, "Now that we have captured the clinical trial market in early phase trials we are excited about continuing our network expansion in to later phase clinical trials across North America."
About Target Health:
Target Health Inc. is a New York City based full service e*CRO with staff dedicated to all aspects of Regulatory Affairs, Clinical Research, Biostatistics, Data Management, Medical Writing, Strategic Planning and Drug and Device Development. In addition, Target Health has developed innovative web-based software tools that provide its clients with a significant productivity edge. Products include Target e*CRF (EDC); Target Document(r) (eTMF); Target e*Pharmacovigilance (SAE management); and Target e*CTR(r) (eClinical Trial Record; eSource) which is equivalent to electronic health record for clinical trials in that the clinical trial data are entered directly into an electronic data capture system at the time of the office visit. Target Health Inc. represent over 30 companies at FDA and submits approximately 3 original INDs per year. Clients include small to medium size as well as Fortune 100 companies. There are now 24 products marketed world-wide that used Target e*CRF for their pivotal trials.
About Verified Clinical Trials
Verified Clinical Trials is a forward thinking company developed by experts in the clinical research community to proactively improve research subject safety and data quality in clinical research trials. Verified Clinical Trials halts dual enrollment in clinical trials and defines itself as the world's leader in the field of database registries in clinical trial research. Verified Clinical Trials is the only clinical research database registry that is fully web based and designed specifically to enhance the quality of both early and late phase trials and has the scalability to reach all sites nationally and globally. Verified Clinical Trials is a HIPAA- and 21 CFR part 11- compliant online subject registry to anonymously and securely validate subjects and prevent dual enrollment in multiple concurrent research studies. Verified Clinical Trials offers numerous other value-added services to the clinical research site, CRO, and pharmaceutical sponsor, that prove invaluable with regards to financial and legal issues and liabilities. To RSVP or for more information, visit http://www.verifiedclinicaltrials.com.
Contact For Verified Clinical Trials
Kerri Weingard, ANP, Chief Operating Officer
Verified Clinical Trials +1 516 998-7499