WCCT Global and Verified Clinical Trials have collaborated to developed a novel dosing reminder module to their arsenal of tools to improve clinical research safety and data quality.
Costa Mesa, CA (PRWEB) January 02, 2013
WCCT Global and Verified Clinical Trials have collaborated and have developed a novel dosing reminder module to their arsenal of tools to improve clinical research safety and data quality. VCT is North America's largest clinical trials database registry that prevents dual enrollment in clinical trials. VCT continually adds new features to attract early and late phase companies and trials to their network. The world's largest pharmaceutical companies, CROs, and research units employ the Verified Clinical Trials system to enhance and validate patient reported data to ensure data integrity.
WCCT Global, a Full Service Contract Research Organization (CRO) supporting Phase I - IV biopharmaceutical and device development has collaborated with Verified Clinical Trials (VCT), the largest national clinical trials database in the US to help them enhance the capabilities of the VCT Database Registry system. This new enhancement designed in collaboration with WCCT enables the investigator to document study-participant adherence to medication schedules. Mel Affrime, Sr. VP R&D, WCCT said, “Patient adherence to clinical research protocol procedures is critical along with returning to the investigational site for study procedures and safety assessments. This added enhancement now offered by VCT adds another level of security in the validity of the data that we capture for our clients”.
Mitchell Efros, MD, FACS, CEO and President of Verified Clinical Trials, stated "The recent released study medication adherence reminder system will improve dosing compliance in clinical trials. The module has the ability to remind the research volunteer to take the medication directly through the VCT registry. There is also the option of having the research subject respond to the reminder signaling their compliance and execution of the required dosing. WCCT Global, one of the early subscribers to our database, has always been an industry leader in their efforts to ensure the safety of their study participants and the quality of their clinical data. It has been a pleasure working with the WCCT team to make this enhancement available to our entire network of subscribers.”
About WCCT Global
WCCT Global is a multi-site, full service global contract research organization (CRO) of outsourced early drug development and late phase services to the pharmaceutical, biotechnology and medical device industries. The WCCT Global vision, “With compassion for people, we strive for tomorrow's therapies to be available today” truly exemplifies the focus and reason for our cutting edge work both in our clinics and throughout our operations. As a drug development partner, WCCT Global collaborates with domestic and foreign innovator companies who need regulatory, program management, data management and strategic consulting support, with an emphasis on overseeing and executing trials in special disease populations, ethno-bridging, and cardiac safety. In addition, WCCT has extensive experience with healthy volunteer studies including First-in-Human (FIH), as well as specific therapeutic expertise in Allergy, Asthma, Infectious Disease, Pediatric, Ophthalmology, Oncology, Renal, and Vaccines. Visit WCCT Global on the web at http://www.wcct.com.
About Verified Clinical Trials:
Verified Clinical Trials was 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 clinical trial database registries. 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 value-added services to the clinical research site, CRO, and pharmaceutical sponsor that prove invaluable with regards to financial and legal issues and liabilities.
For more information, visit http://www.verifiedclinicaltrials.com.
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