{"product_id":"eu-clinical-trial-regulation-eu-ctr-requirements-2026-12-17","title":"EU Clinical Trial Regulation (EU-CTR) Requirements","description":"\u003cp class=\"header-block-grey\"\u003eCourse Description\u003c\/p\u003e\u003cp\u003eThe EU Clinical Trial Regulation (Regulation (EU) No. 536\/2014) has ushered in a transformative era for clinical trials within the European Union and is built on three fundamental pillars: Enhancing the efficiency of clinical trials in Member States Concerned (MSCs) to foster innovation and reduce duplication, increasing the transparency of clinical trials across Europe, and prioritizing participant safety. At the core of this regulatory shift is the Clinical Trial Information System (CTIS), which serves as the central hub for all submissions to the EU. This comprehensive web seminar is designed to provide participants with a thorough understanding of the EU-CTR, its objectives, and its practical implications for clinical trial conduct in the EU. \u003c\/p\u003e\u003cp class=\"header-block-grey\"\u003eLearning Objectives\u003c\/p\u003e\u003cul type=\"disc\"\u003e \u003cli\u003eUnderstand the rationale and requirements for the regulation\u003c\/li\u003e \u003cli\u003eBecome proficient in identifying and comprehending the different types of submissions within CTIS\u003c\/li\u003e \u003cli\u003eExplore the critical roles and responsibilities of key stakeholders involved\u003c\/li\u003e \u003cli\u003eGain a comprehensive understanding of the submission process through the CTIS, from initial registration to ongoing updates and amendments\u003c\/li\u003e \u003c\/ul\u003e\u003cp class=\"header-block-grey\"\u003eWho Should Attend\u003c\/p\u003e\u003cul type=\"disc\"\u003e \u003cli\u003eClinical Trial Management, Monitors and Leads\u003c\/li\u003e \u003cli\u003eRegulatory Affairs\u003c\/li\u003e \u003cli\u003eExecutive Management\u003c\/li\u003e \u003c\/ul\u003e\u003cp class=\"header-block-grey\"\u003eInstructor\u003c\/p\u003e\u003cp\u003eAndy Lawton\u003c\/p\u003e\u003cp\u003e\u003ca href=\"https:\/\/www.barnettinternational.com\/instructor-biographies\" title=\"Click here for complete trainer biographies\" style=\"font-family:inherit;font-size:inherit;text-align:inherit;text-transform:inherit;white-space:inherit;word-spacing:normal;\"\u003eClick here for complete trainer biographies\u003c\/a\u003e\u003c\/p\u003e\u003cp class=\"header-block-grey\"\u003eRegistration Fees\u003c\/p\u003e\u003cp\u003e$735*\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 hours (0.1 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#: 0778-0000-24-034-L99-P. Released: 2\/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":53375366070637,"sku":"BI17596","price":735.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/www.barnettinternational.com\/products\/eu-clinical-trial-regulation-eu-ctr-requirements-2026-12-17","provider":"Barnett International ","version":"1.0","type":"link"}