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DTSTART:19700308T020000
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UID:2140535:Event:453516
DTSTAMP:20260413T123946Z
SUMMARY:The Drug Development Process from Concept to Market
DESCRIPTION:This course is designed to cater for employees of pharmace
 utical companies who would like an understanding of the drug developme
 nt and regulatory approval process. The course starts by considering t
 he global pharmaceutical market, important therapeutic areas and the r
 oles of different pharmaceutical professionals in the development proc
 ess, as well as a definition of drugs and medical devices. The drug de
 velopment process, from discovery to post-marketing surveillance, is t
 hen explained. Topics include the identification of drug targets, synt
 hesis of chemical drugs and the development of biologics, pharmacokine
 tics and toxicity screening, pre-clinical development, clinical studie
 s, regulatory submissions, managing post-approval change, pharmacovigi
 lance and an overview of regulations governing drug manufacture and di
 stribution.\n\nFor more information visit https://medtechiq.ning.com/e
 vents/the-drug-development-process-from-concept-to-market
DTSTART;TZID=America/New_York:20210209T100000
DTEND;TZID=America/New_York:20210209T170000
CATEGORIES:seminae
LOCATION:online
WEBSITE:https://www.complianceonline.com/drug-development-process-conc
 ept-and-market-seminar-training-80635SEM-prdsm?channel=MedTech%20I.Q
URL:https://www.complianceonline.com/drug-development-process-concept-
 and-market-seminar-training-80635SEM-prdsm?channel=MedTech%20I.Q
CONTACT:8887172436
ORGANIZER;CN=ComplianceOnline:https://medtechiq.ning.com/profile/Refer
 ral512
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 /file/get/8499677259?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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