![]() ![]() Patient level data for researchers, and full references for clinical and preclinical publications. The GSK Study Register includes protocol summaries, scientific results summaries, plain language results summaries, full protocols, analysis plans, clinical study reports, regulatory overview documents, Supports external physician and primary care centre representative requests for compassionate use of GSK and ViiV Healthcare medicines.Ī repository of data and information from GSK studies. Investigational Product (IP) shipments will have a Temperature Monitor (TempTracer) monitoring the internal temperature of a shipment of medication.ĭuring any type of disaster the CSHD can be a point of contact for Investigators.įDA owned web-site listing all trials for all potential drugs in the US market for public access.Įuropean version of ct.gov listing trials for all potential drugs for the EU market. The system for registering subjects, reporting visits, and allocating study medication. Inform non SSO studies or direct link without study number.The electronic case report form used for most GSK studies. The software unifies electronic data capture (EDC), auto-coding, and study data forms optimization, enabling complete control over trials configuration and management. Redefines data management to help medtech clinical teams manage today's trials with agility and speed. Trial Master File), CTMS (Clinical Trial Management System), SRD (Safety Report Distribution) and CDMS (Clinical Data Management Suite) onto a single cloud platform, to optimize execution of clinical trials and ensure inspection It unifies clinical operations and data management systems including SSU (study start up), eTMF (Electronic Veeva Clinical Vault is a cloud enterprise content management platform that tracks critical information from product development to commercialization. The learning management system used by GSK to deliver web-based training to Investigator Site Staff. ![]() Support Description - Click to Sort by Support Description. "We help our clients to take advantage of technology developments to tackle dynamic regulatory environments, escalating disease complications and fierce competition to get products to the market," said Mr Gopakumar Menon, CEO, Siro.Support Name - Click to Sort by Support Name. "The software's flexibility, scalability and real-time access to trial data will help streamline and accelerate large and complex international trials." Combined with our expertise in clinical development, we can now offer our clients a very effective and seamless user experience," said Mr Khushru Patel, global head, information technology, Siro. By deploying Oracle Health Sciences InForm, we have upgraded our technology platforms to global standards. "Our IT capabilities in the region are second to none. With a breadth of services encompassing clinical operations, clinical data management, medical writing, biostatistics and statistical programming, pharmacovigilance and clinical trial supplies management, this comes as a huge step toward adopting global trial processes, as EDC systems are widely used across western Europe and the US. The application of Oracle Health Sciences InForm enables Siro to automate and streamline solutions for the global biopharma and medical devices companies in their clinical development process across therapeutic areas and phases. The project is an integrated life sciences solution that consists of all the tools required to efficiently conduct and manage electronic data capture (EDC)-based clinical trials. Singapore: Siro Clinpharm, a leading full service clinical research organization, has deployed one-of-the-biggest IT advancement projects in the Asia Pacific region, Oracle Health Sciences InForm.
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