The European Clinical Quality Oversight Forum offers an in-depth education on risk-based approaches for selecting, managing and monitoring clinical vendors and sites. The forum attracts senior-level clinical quality and operations professionals from leading pharma, biotech and device companies of varying size, making it an ideal event for networking and forming new business relationships. For additional information on sponsoring or exhibiting opportunities, contact Justin Kreamer at 917-932-0429 or email@example.com.
CluePoints® is a Risk-Based Monitoring and Central Statistical Monitoring solution that has been designed and perfected over the last 15 years. It employs unique statistical algorithms to determine the quality, accuracy, and integrity of clinical trial data both during and after study conduct. Aligned with guidance from the ICH, FDA, and EMA, CluePoints® is deployed to support traditional on-site monitoring, medical review and to drive a Risk-Based Monitoring strategy.
Navitas, the dedicated life sciences company of TAKE Solutions, harnesses the combined knowledge and experience of three legacy companies—Ecron Acunova, Navitas, and Intelent—to provide end-to-end services and solutions. We help our clients address their most critical problems by bringing together the capabilities of a full-service CRO, a technology-led life sciences services provider across clinical, regulatory and safety, and a life sciences big data services and analytics provider.
RiverArk is a global consultancy offering services within QA and QM and PV domain. Our clients include Pharmaceutical, Biotech, and Medical Device companies. We provide GxP auditing, QM consulting, Inspection readiness services, GAP analysis, Risk assessment & mitigation and GxP training.
RiverArk has a global team of 20 highly qualified GxP auditors who strive to provide valuable, in-depth consulting, auditing and training across the industry. With varied backgrounds, multinational positioning, wide-ranging training and industry experience, our consultants are well suited to provide expertise, skills, and objectivity to evaluate, build or improve your quality systems & compliance.
TRI are a business solutions provider, entirely focused on quality management, risk-based monitoring (RBM) and ICH GCP E6 Rev2 compliance. TRI developed the world’s first dedicated RBM platform, OPRA. OPRA is a cloud-based, per-study platform which can be tailored to the needs of any trial and data source. TRI provide the technology, services, and training required to efficiently enable any company running clinical trials in RBM and ICH CGP E6 Rev2 compliance.