Latest news with #VerifiedClinicalTrials
Yahoo
08-07-2025
- Health
- Yahoo
Verified Clinical Trials Launches in Japan in Partnership with Medical Revolutions Japan (MRJ) and JACIC to Prevent Duplicate and Professional Subjects in Clinical Trials
TOKYO & GARDEN CITY, N.Y., July 08, 2025--(BUSINESS WIRE)--Verified Clinical Trials (VCT), the global leader in clinical trial subject registry solutions, has officially launched operations in Japan through a collaboration with Medical Revolutions Japan (MRJ) and the Japan Association of Contract Institutes for Clinical Pharmacology (JACIC) to address the growing global challenge of duplicate and professional research subjects in clinical trials. For the past thirty years, Japan's only system for preventing duplicate subject registration was developed by JACIC and used across Phase 1 studies. However, a recent review concluded that the system requires substantial modernization to meet international standards and support the growing number of global clinical trials. In addition, duplicate subjects in clinical trials have become a growing concern in Phase II and Phase III trials as well. After extensive evaluation, the VCT platform—widely adopted as the global standard—was selected as the best solution and replacement. With the support of MRJ, which was commissioned by JACIC to assist with domestic implementation, Verified Clinical Trials has begun initiating sites in Japan, with additional sites expected to join in the coming weeks and months. These sites will benefit from the biometric capabilities of the VCT system, offering a higher level of subject authentication and protocol compliance. This rollout will include sites conducting Phase I through Phase IV clinical trials. "Given the sophisticated functionality and biometric identification capability of the VCT system, as well as its proven match for other Asian countries," a representative of MRJ commented, "I believe it is destined to become the new Japan standard for duplicate subject registration prevention." Verified Clinical Trials brings to Japan a cross-sponsor, cross-therapeutic area subject registry already in use in up to 40 countries. The platform not only detects but also prevents duplicate subjects and other protocol violations at the time of screening—and maintains protections throughout the entire duration of the trial. "We're honored to bring VCT to Japan as part of a shared mission to raise the standard of subject protection and trial integrity," said Mitchell Efros, MD, President and CEO of Verified Clinical Trials. "No clinical trial or geography is immune to the challenge of duplicate subjects—it's a global phenomenon. Our system provides an effective, scalable solution." "By introducing VCT in Japan, sponsors gain a real-time tool to proactively manage protocol risk and ensure only qualified participants are enrolled," added Kerri Weingard, ANP, Vice President and Chief Operating Officer of Verified Clinical Trials. "This launch represents our commitment to regulatory excellence and regional partnership across the APAC region," said Eve Hsu, Global Regulatory Director at Verified Clinical Trials. "With dedicated team members based throughout APAC, we're well-positioned to support sites and sponsors locally and help elevate clinical trial quality and compliance across the region." The VCT system was co-founded by Mitchell Efros, MD, and Kerri Weingard, ANP, both experienced clinical researchers who developed the registry to address long-standing challenges in subject eligibility, data quality, and compliance. About Verified Clinical Trials (VCT)Verified Clinical Trials is the world's largest research subject database registry designed to detect and prevent duplicate and professional subjects in clinical trials. VCT fills a critical gap in the clinical research industry by providing insight into a research subject's past trial participation. This enables better subject selection and helps ensure successful clinical trial execution. Active in up to 40 countries, VCT supports sponsors, CROs, and research sites across all trial phases and therapeutic areas, enhancing data quality, subject safety, and protocol compliance. About Medical Revolutions Japan (MRJ)Medical Revolutions Japan is a clinical trial consultancy managed and staffed by industry experts with long and rich experience in all facets of clinical development and research in the Japanese market. Founded in 2024 as an affiliate of Keikokai Medical Corporation, a longstanding clinical research unit operator in Tokyo, MRJ is currently expanding its global client base and working to connect both international and local players to help the domestic Japanese clinical development industry rise to the challenges brought about by technological disruptions as it continues to grow and internationalize. View source version on Contacts For media inquiries, please contact:connect@ Sign in to access your portfolio
Business Wire
08-07-2025
- Health
- Business Wire
Verified Clinical Trials Launches in Japan in Partnership with Medical Revolutions Japan (MRJ) and JACIC to Prevent Duplicate and Professional Subjects in Clinical Trials
TOKYO & GARDEN CITY, N.Y.--(BUSINESS WIRE)-- Verified Clinical Trials (VCT), the global leader in clinical trial subject registry solutions, has officially launched operations in Japan through a collaboration with Medical Revolutions Japan (MRJ) and the Japan Association of Contract Institutes for Clinical Pharmacology (JACIC) to address the growing global challenge of duplicate and professional research subjects in clinical trials. 'No clinical trial or geography is immune to the challenge of duplicate subjects—it's a global phenomenon. Our system provides an effective, scalable solution.' For the past thirty years, Japan's only system for preventing duplicate subject registration was developed by JACIC and used across Phase 1 studies. However, a recent review concluded that the system requires substantial modernization to meet international standards and support the growing number of global clinical trials. In addition, duplicate subjects in clinical trials have become a growing concern in Phase II and Phase III trials as well. After extensive evaluation, the VCT platform—widely adopted as the global standard—was selected as the best solution and replacement. With the support of MRJ, which was commissioned by JACIC to assist with domestic implementation, Verified Clinical Trials has begun initiating sites in Japan, with additional sites expected to join in the coming weeks and months. These sites will benefit from the biometric capabilities of the VCT system, offering a higher level of subject authentication and protocol compliance. This rollout will include sites conducting Phase I through Phase IV clinical trials. 'Given the sophisticated functionality and biometric identification capability of the VCT system, as well as its proven match for other Asian countries,' a representative of MRJ commented, 'I believe it is destined to become the new Japan standard for duplicate subject registration prevention.' Verified Clinical Trials brings to Japan a cross-sponsor, cross-therapeutic area subject registry already in use in up to 40 countries. The platform not only detects but also prevents duplicate subjects and other protocol violations at the time of screening—and maintains protections throughout the entire duration of the trial. 'We're honored to bring VCT to Japan as part of a shared mission to raise the standard of subject protection and trial integrity,' said Mitchell Efros, MD, President and CEO of Verified Clinical Trials. 'No clinical trial or geography is immune to the challenge of duplicate subjects—it's a global phenomenon. Our system provides an effective, scalable solution.' ' By introducing VCT in Japan, sponsors gain a real-time tool to proactively manage protocol risk and ensure only qualified participants are enrolled,' added Kerri Weingard, ANP, Vice President and Chief Operating Officer of Verified Clinical Trials. 'This launch represents our commitment to regulatory excellence and regional partnership across the APAC region,' said Eve Hsu, Global Regulatory Director at Verified Clinical Trials. 'With dedicated team members based throughout APAC, we're well-positioned to support sites and sponsors locally and help elevate clinical trial quality and compliance across the region.' The VCT system was co-founded by Mitchell Efros, MD, and Kerri Weingard, ANP, both experienced clinical researchers who developed the registry to address long-standing challenges in subject eligibility, data quality, and compliance. About Verified Clinical Trials (VCT) Verified Clinical Trials is the world's largest research subject database registry designed to detect and prevent duplicate and professional subjects in clinical trials. VCT fills a critical gap in the clinical research industry by providing insight into a research subject's past trial participation. This enables better subject selection and helps ensure successful clinical trial execution. Active in up to 40 countries, VCT supports sponsors, CROs, and research sites across all trial phases and therapeutic areas, enhancing data quality, subject safety, and protocol compliance. About Medical Revolutions Japan (MRJ) Medical Revolutions Japan is a clinical trial consultancy managed and staffed by industry experts with long and rich experience in all facets of clinical development and research in the Japanese market. Founded in 2024 as an affiliate of Keikokai Medical Corporation, a longstanding clinical research unit operator in Tokyo, MRJ is currently expanding its global client base and working to connect both international and local players to help the domestic Japanese clinical development industry rise to the challenges brought about by technological disruptions as it continues to grow and internationalize.
Business Wire
22-04-2025
- Business
- Business Wire
Verified Clinical Trials Achieves ISO/IEC 27001 Certification, Reinforcing Commitment to Data Security and Integrity in Clinical Research To Prevent Duplicate Subjects In Clinical Trials
BUSINESS WIRE)-- Verified Clinical Trials (VCT), the world's largest global research subject database designed to prevent dual enrollment in clinical trials with duplicate research subjects and protocol violations in clinical trials, proudly announces it has achieved ISO/IEC 27001 certification, the international gold standard for information security management systems (ISMS). Verified Clinical Trials (VCT), the world's largest global research subject database designed to prevent dual enrollment in clinical trials This significant milestone reflects VCT's ongoing dedication to the highest levels of data privacy, security, and operational excellence across its global platform, which supports pharmaceutical companies, clinical research organizations (CROs), and investigative sites. 'ISO 27001 certification is a landmark achievement for VCT,' said Kerri Weingard, Co-Founder, VP and Global COO. 'Our clients trust us with highly sensitive and regulated data. This certification reaffirms that we operate with the most stringent controls to protect that data and the integrity of the research process itself.' VCT plays a critical role in ensuring research subject compliance by preventing fraudulent and duplicate enrollment in clinical trials, thereby safeguarding protocol fidelity and participant safety. The company's proprietary technology and global centralized research subject registry is used by countless sponsors of clinical trials and in tens of thousands of research sites globally, across all phases of clinical research and therapeutic areas. 'Achieving ISO 27001 status validates the robustness of our internal systems and processes,' said Palani Masilamani, CTO of Verified Clinical Trials. 'It demonstrates that information security is embedded into the DNA of our technology and operations. This is a win not only for VCT but for every sponsor and site that depends on our platform.' The rigorous ISO/IEC 27001 certification process, conducted by an accredited third-party auditor, required VCT to demonstrate an ongoing and systematic approach to managing sensitive company and customer information. The standard outlines best practices in information security risk management, access control, incident response, and data protection policies. 'This accomplishment reflects our team's tireless efforts and unwavering commitment to excellence,' added Mitchell Efros, Co-Founder and CEO of Verified Clinical Trials. 'ISO certification enhances the trust we've built with clients and partners around the world and positions us for continued innovation and leadership in clinical trial compliance.' With ISO 27001 certification in place, VCT continues to lead the way in promoting integrity and safety in clinical trials, while meeting the evolving regulatory and cybersecurity expectations of the life sciences industry. Verified Clinical Trials continues to lead the industry with the only global cross-sponsor, cross-therapeutic solution that both detects and prevents protocol violations in real-time at the time of screening. Now backed by ISO certification, VCT offers an even stronger foundation for research integrity and stakeholder trust across the globe. About Verified Clinical Trials Verified Clinical Trials (VCT) is the largest and most comprehensive global research subject database to prevent dual enrollment in clinical trials and protocol deviations in clinical trials. Used by leading pharmaceutical companies, CROs, and research sites worldwide, VCT is a trusted partner in improving subject safety, data quality, and regulatory compliance.
