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DTSTART:19700308T020000
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UID:2140535:Event:468730
DTSTAMP:20260601T014012Z
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.\nLearning Objectives:\nBy the end of this course, you will
  understand:\n\nThe size of the global pharmaceutical market and the k
 ey therapeutic areas being addressed by innovator companies\nThe roles
  of different pharmaceutical professionals\nTypical costs and timeline
 s associated with drug development\nHow new drugs are developed agains
 t targets in the human body\nReasons why drugs fail during development
 \nFactors affecting oral bioavailability\nHow drugs are screened for t
 oxicity\nThe potential influence of polymorphism, salt form and isomer
 ism on efficacy and safety\nHow formulation can affect drug performanc
 e\nHow the safety and efficacy of drug products are ensured during QC 
 release testing\nThe information obtained at each stage of clinical re
 search\nThe structure of regulatory submissions\n\nWho will Benefit:\n
 \nNon-scientific employees of pharmaceutical companies who would like 
 to understand how drugs are developed (e.g. IT, human resources, engin
 eering and administrative staff)\nRecently-appointed scientific staff 
 with no previous experience of the pharmaceutical industry\nAny pharma
 ceutical employee wishing to improve their knowledge of drug developme
 nt\n\n\nFor more information visit https://medtechiq.ning.com/events/t
 he-drug-development-process-from-concept-to-market-1
DTSTART;TZID=America/New_York:20210727T100000
DTEND;TZID=America/New_York:20210727T170000
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
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/9025713658?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc
 eOnline:https://medtechiq.ning.com/profile/Referral512
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