{"product_id":"managing-epro-in-clinical-trials","title":"Managing ePRO in Clinical Trials","description":"\u003cp\u003e\u003cstrong\u003eManaging ePRO in Clinical Trials - TTC KW C07\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe \u003cstrong\u003eManaging ePRO in Clinical Trials\u003c\/strong\u003e course is designed for professionals who plan, source, build or run the ePRO component of a clinical trial and want a clear, practical way to get it right. It is suitable for \u003cstrong\u003eintermediate learners\u003c\/strong\u003e in clinical research, including \u003cstrong\u003eClinical Data Managers, Clinical Trial Managers, Project and Vendor Managers\u003c\/strong\u003e, and professionals working in \u003cstrong\u003eclinical operations, biometrics, quality assurance, or related functions\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003eThis course follows the life of an ePRO trial \u003cstrong\u003estep by step, across four stages\u003c\/strong\u003e: decide and design, source and contract, build and prepare, and run and close. Rather than treating ePRO as a one-size-fits-all recipe, the module walks every step of the timeline, showing \u003cstrong\u003ewhen each step happens, whether it applies to your trial, what to decide and document, and the classic pitfalls\u003c\/strong\u003e, all illustrated with one running example trial to keep the decisions concrete.\u003c\/p\u003e\n\u003cp\u003eIn a regulated clinical research environment, ePRO data is mostly live and mostly the source, so the design and operational choices decide the quality of the evidence. This module helps you understand \u003cstrong\u003ewhat to settle in the protocol rather than the build\u003c\/strong\u003e, \u003cstrong\u003ehow to close the gaps between sponsor, CRO and vendor\u003c\/strong\u003e, and how to keep investigator control and compliance intact, so you can run an ePRO trial that holds up to scrutiny.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eWhy Learn with TriTiCon\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eTriTiCon delivers \u003cstrong\u003eclinical development training\u003c\/strong\u003e based on extensive hands-on experience from real clinical trials and operational roles across sponsors, CROs, and life sciences organisations. The content is developed by professionals who understand both the opportunities and the constraints of working in a regulated environment.\u003c\/p\u003e\n\u003cp\u003eIn the context of ePRO, this practical perspective is essential. While many resources cover the technology in the abstract, TriTiCon focuses on \u003cstrong\u003ehow an ePRO trial actually runs\u003c\/strong\u003e, including instrument licensing, devices and fallback, the three-player gap between sponsor, CRO and vendor, compliance, data changes, and close-out with investigator access.\u003c\/p\u003e\n\u003cp\u003eThe C07 module is built around a concrete, step-by-step timeline, with a running example trial throughout, \u003cstrong\u003eshowing where ePRO trials typically go wrong and how to avoid it\u003c\/strong\u003e. You will see how to make and document the right decisions at each step, from the first ePRO-or-not question to decommissioning.\u003c\/p\u003e\n\u003cp\u003eCompared with generic clinical research courses, TriTiCon's training emphasises \u003cstrong\u003ejob-relevant decisions\u003c\/strong\u003e, realistic timelines, and the practical pitfalls that only show up when you actually run an ePRO trial.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eWhat You'll Learn\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThis module provides a structured, end-to-end view of an ePRO trial, from the first design decisions in the protocol to the day the system is switched off. The content is organised into four stages that build from deciding and designing, through sourcing and contracting, to building, running and closing the trial.\u003c\/p\u003e","brand":"TriTiCon","offers":[{"title":"Default Title","offer_id":50874852016176,"sku":"TTC-KW-C07","price":46.0,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0661\/1628\/8560\/files\/C07-With-Text.jpg?v=1792749312","url":"https:\/\/www.triticon.com\/products\/managing-epro-in-clinical-trials","provider":"TriTiCon","version":"1.0","type":"link"}