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:82336 DTSTAMP:20260526T135930Z SUMMARY:Seminar on Phase I GMPs | Drug Development Course DESCRIPTION: \nCourse \"Seminar on Phase I GMPs\" has been pre-approv ed by RAPS as eligible for up to 12 credits towards a participant's RA C recertification upon full completion.\nDescription:\nEarly clinical trials are conducted to establish initial safety of a drug. The studie s are generally in small number of healthy subjects and use lower dose s of the drug product. Therefore, only small amounts of investigationa l material are required. In order to not undertake substantial costs a nd to reduce regulatory burden during these early stages, the FDA has established guidelines to allow early stage investigational products t o be manufactured under less stringent GMPs.\nThis workshop will revie w the current regulations, guidance documents for early stage manufact uring and GMPs in detail. Regulatory strategies and logistical conside rations for early development stage product, including vendor selectio n and management, stability, labeling, and documentation requirements will also be reviewed and explored.\nWhy Should you Attend:\nAttend th is conference so that you may understand differences between GMP requi rements for early and later stage clinical development. Explore and di scuss ways to develop and implement strategies for early GMPs for phas e I clinical studies.\n\nLocation:  Philadelphia, PA Date: April 16th & 17th, 2019 and Time 9:00 AM to 6:00 PM\nVenue: DoubleTree by Hilton Philadelphia Airport, 4509 Island Avenue, Philadelphia, PA 19153\n \ nPrice:\n1 ATTENDEE $2,000, Regular Price: $2000, Register for 1 atten dee\n5 ATTENDEES $10,000, Regular Price: $10,000, Register for 5 atten dees\n10 ATTENDEES $20,000, Regular Price: $20,000, Register for 10 at tendees\nUntil March 10, Early Bird Price: $2,000. From March 11 to April 12, Regular Price: $2,200.\nUse this promo code GCP50 to get 50 % off.\n \nSponsorship Program benefits for seminarFor More Informati on-\n\n \nContact us today!\nNetZealous LLC DBA GlobalCompliancePanel \nglobalcompliancepanel@gmail.com\nToll free: +1-800-447-9407\nPhone: +1-510-584-9661\nWebsite:\n \nRegistration Link -\nFollow us on Linke dIn:\nLike us our Facebook page:\nFollow us on Twitter:\n \n \n \n  \n\nFor more information visit https://medtechiq.ning.com/events/semi nar-on-phase-i-gmps-drug-development-course DTSTART;TZID=America/New_York:20190416T090000 DTEND;TZID=America/New_York:20190417T180000 CATEGORIES:seminar, on, phase, i, gmps LOCATION:DoubleTree by Hilton Philadelphia Airport, 4509 Island Avenue , Philadelphia, PA 19153 WEBSITE:https://www.globalcompliancepanel.com/seminar/seminar-on-phase -I-GMPs-901939SEMINAR?medtechiq-*SEO URL:https://www.globalcompliancepanel.com/seminar/seminar-on-phase-I-G MPs-901939SEMINAR?medtechiq-*SEO CONTACT:800-447-9407 ORGANIZER;CN="John Robinson":https://medtechiq.ning.com/profile/JohnRo binson ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0 /file/get/1056581094?profile=original ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="John Rob inson":https://medtechiq.ning.com/profile/JohnRobinson END:VEVENT END:VCALENDAR