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Inform edc3/30/2023 GSK Electronic Cell Tracking System (eCellTS)Ī global Cell Orchestration application enabling the tracking of patients cells throughout the supply chain and manufacturing of Cell and Gene Therapy productsĬlinical Study Data entered in a Tabulation Model used for statistical analysis Involves extracting container codes from one application to create a list of all medications dispensed to each site so CRAs can check the report output against what is remaining at the end of the clinical trial. These studies are also known as Investigator-Initiated Studies, Investigator-Initiated-Trials, Investigator Initiated Research or Investigator Sponsored Research. Supported Studies are research conducted by an external Sponsor with GSK's support. Patient level data for researchers, and full references for clinical and preclinical publications.Ī web-based system used for tracking study recruitment. 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. The system used by Primary Investigator’s to access and/ or query invoices/payments for Studies they are associated with. Used to collect pictures or documents related to GSK Vaccines Studies.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. Source Data Base for Internet Randomization Investigational Product (IP) shipments will have a Temperature Monitor (TempTracer) monitoring the internal temperature of a shipment of medication. The system for registering subjects, reporting visits, and allocating study medication. It enables the user to record patient information (ie, visit, lab, and adverse event data) using forms that are customized for Is a cloud–based clinical data management system used to electronically capture, manage, and report clinical research data. 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. Support Name - Click to Sort by Support Name.
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