BEGIN:VCALENDAR PRODID:NingEventWidget-v1 VERSION:2.0 METHOD:PUBLISH BEGIN:VTIMEZONE TZID:America/New_York X-LIC-LOCATION:America/New_York BEGIN:DAYLIGHT TZOFFSETFROM:-0500 TZOFFSETTO:-0400 TZNAME:EDT DTSTART:19700308T020000 RRULE:FREQ=YEARLY;BYMONTH=3;BYDAY=2SU END:DAYLIGHT BEGIN:STANDARD TZOFFSETFROM:-0400 TZOFFSETTO:-0500 TZNAME:EST DTSTART:19701101T020000 RRULE:FREQ=YEARLY;BYMONTH=11;BYDAY=1SU END:STANDARD END:VTIMEZONE BEGIN:VEVENT UID:2140535:Event:63146 DTSTAMP:20260530T035244Z SUMMARY:Best Practices for Clinical Trial Site Selection - Finding Hig h-Enrolling, High-Data Quality Producing Sites DESCRIPTION:This clinical compliance training will provide attendees b est practices for clinical trial site selection. Attendees will learn how to identify high-quality and low-quality data sites and how to add ress issues in both of those scenarios.\n\nWhy Should You Attend:\nCli nical trial site enrollment rate is often the leading factor in determ ining study length and associated costs with getting product to the ma rket. Most large-scale trials involve a typical ratio of 25% of sites enrolling 75% of the study subjects, 25% enroll no subjects, and the r emaining 50% enroll the remainder of subjects. With limited budgets an d timelines, there are proven methods which virtually eliminate the no n-enrolling sites and move them to high or near-high enrolling sites, which is crucial when there is a limited number of sites to work with due to budgetary and other constraints. With estimated start-up costs currently averaging $30,000 per site, it is crucial that high-enrollin g, high-quality sites are selected. This process works for both trials run completely within the US and for trials on a global basis. Howeve r, there are some differences in procedures that must be followed when identifying sites outside of the US.\nThis webinar will cover a step- by-step procedure to identify high-enrolling sites for clinical trials . It will help the attendees to quickly identify low-enrolling sites t o either remove them from the study or bring them up-to-speed. It will also explain the role of various departments in clinical trial site s election.\nAreas Covered in the Webinar:\n\nA step-by-step procedure t o identify high-enrolling sites for clinical trials.\nHow to identify which countries and sites are the most suitable for conducting trials outside of the US.\nDetermining cost to benefit of enrolling within va rious countries and between investigators.\nDetermining the impact to the cost of development of the investigational product to the company using various enrollment scenarios.\nHow to quickly identify low-enrol ling sites to either remove them from the study or bring them up-to-sp eed.\nHow to quickly identify high-quality and low-quality data sites and how to address issues in both of those scenarios.\nRole of various departments in clinical trial site selection.\n\nWho Will Benefit:\nT his webinar will provide valuable assistance to all personnel in:\n\nC linical Operations within the pharmaceutical, medical device or diagno stics clinical\nBusiness Development\nRegulatory Affairs\nAll personne l within the company with an interest of conducting clinical trials mo re efficiently at overall lower costs with higher quality data\n\nInst ructor Profile:\nAdam Ruskin, PhD, DVM, MPH is the founder of LabCRO, Inc., one of California's largest Clinical Research Organizations. Dr . Ruskin was a researcher at the Centers for Disease Control (CDC), an FDA Advisor, and two-time TEDMED award nominee for innovation. He is the creator of LabTracker, the industry's first system for tracking cl inical trial samples from the time of patient sampling until result po sting. He has lead all clinical, data management and biostatistics act ivities at 4 successful start-up pharmaceutical, biotech, and medical device and diagnostics companies, and now leads successful clinical an d data management teams for his clients through LabCRO. As a leading i ndustry speaker for over 20 years, he knows the details of what it tak es to get investigational products approved, especially under required budgets and timelines of most companies.\n\nFor more information visi t https://medtechiq.ning.com/events/best-practices-for-clinical-trial- site-selection-finding-high-1 DTSTART;TZID=America/New_York:20140213T100000 DTEND;TZID=America/New_York:20140213T111500 CATEGORIES:clinical LOCATION:Online Event WEBSITE:http://www.complianceonline.com/ecommerce/control/trainingFocu s/~product_id=703250?channel=medtechiq URL:http://www.complianceonline.com/ecommerce/control/trainingFocus/~p roduct_id=703250?channel=medtechiq CONTACT:+1-650-620-3915 ORGANIZER:ComplianceOnline ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/ file/get/2562006613?profile=original ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc eOnline:https://medtechiq.ning.com/profile/Referral512 END:VEVENT END:VCALENDAR