{"product_id":"database-design-considerations-in-clinical-trials-2026-12-10","title":"Database Design Considerations in Clinical Trials","description":"\u003cp class=\"header-block-grey\"\u003eCourse Description\u003c\/p\u003e\u003cp\u003eThis web seminar will identify the nine steps necessary to plan the data collection required as contained in the study protocol and other aspects of the clinical trial. Prioritizing the data and recognition of the risk assessment process will be covered in detail, as well as the identification of data standards. Data standards will be discussed and the relationship between CDASH and CDISC will be introduced. Database design considerations, including the elements to be included along with the most advantageous formation of the data capture for database elements (database questions, database answers, and the different element types) are also covered. Additionally, some examples of physical database design will be featured.\u003c\/p\u003e\u003cp class=\"header-block-grey\"\u003eLearning Objectives\u003c\/p\u003e\u003cul type=\"disc\"\u003e \u003cli\u003eDetermine data collection requirements based on the protocol\u003c\/li\u003e \u003cli\u003eEvaluate the priority of data required\/risk assessment\u003c\/li\u003e \u003cli\u003eIdentify data standards\u003c\/li\u003e \u003cli\u003eDiscuss the relationship between CDASH and CDISC\u003c\/li\u003e \u003c\/ul\u003e\u003cp class=\"header-block-grey\"\u003eWho Should Attend\u003c\/p\u003e\u003cul type=\"disc\"\u003e \u003cli\u003eClinical Database Programmers\u003c\/li\u003e \u003cli\u003eClinical Data Managers\u003c\/li\u003e \u003c\/ul\u003e\u003cp class=\"header-block-grey\"\u003eInstructor\u003c\/p\u003e\u003cp\u003eDenise G. Redkar-Brown, MT\u003c\/p\u003e\u003cp\u003e\u003cspan class=\"purple-link\"\u003e\u003ca href=\"https:\/\/stage.barnettinternational.com\/instructor-biographies\" title=\"Click here for complete trainer biographies\"\u003eClick here for complete trainer biographies\u003c\/a\u003e\u003c\/span\u003e\u003c\/p\u003e\u003cp class=\"header-block-grey\"\u003eRegistration Fees\u003c\/p\u003e\u003cp\u003e$835*\u003c\/p\u003e\u003cp\u003e*Includes up to 20 participants per login at a single location. All participants (up to 20) are eligible for \"Certificates of Attendance,\" and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional logins for other locations, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556, or email customer.service@barnettinternational.com for pricing.\u003c\/p\u003e\u003cp class=\"header-block-grey\"\u003eAccreditation Information\u003c\/p\u003e\u003cp\u003eBarnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 1.5 hours (0.15 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion. ACPE#: 0778-0000-24-059-L99-P. Released: 8\/24. \u003c\/p\u003e\u003cp align=\"center\"\u003e\u003cspan class=\"bold\"\u003eHold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471. \u003c\/span\u003e\u003c\/p\u003e","brand":"Barnett International","offers":[{"title":"Commercial","offer_id":53375366463853,"sku":"BI17584","price":835.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/www.barnettinternational.com\/products\/database-design-considerations-in-clinical-trials-2026-12-10","provider":"Barnett International ","version":"1.0","type":"link"}