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TZID:America/New_York
X-LIC-LOCATION:America/New_York
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TZOFFSETFROM:-0500
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TZNAME:EDT
DTSTART:19700308T020000
RRULE:FREQ=YEARLY;BYMONTH=3;BYDAY=2SU
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DTSTART:19701101T020000
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BEGIN:VEVENT
UID:2140535:Event:68786
DTSTAMP:20260519T055719Z
SUMMARY:Webinar on Implementing Best Practices for Global Regulatory I
 ntelligence Programs
DESCRIPTION:Description :\nGlobal regulatory agencies including the Un
 ited States Food and Drug Administration (FDA) review, approve/registe
 r or clear regulatory applications for drugs, biologics and/or medical
  devices including in vitro diagnostic devices (IVDs). It is imperativ
 e that firms identify and map evolving regulatory requirements so that
  regulatory submissions can be better prepared for and managed with aw
 areness in advance.\nThis seminar is intended to discuss the best prac
 tices for implementing Global Regulatory Intelligence (GRI) programs i
 ncluding dos and don’ts. This seminar is further intended to discuss
  how to implement a holistic global regulatory intelligence program su
 itable for your medical product types.\nEstablishing a practical, acti
 onable and sustainable regulatory intelligence program can help an org
 anization save a significant amount of resources (time, efforts and fi
 nancial).\nIn this seminar, the speaker will discuss what firms should
  consider and address when implementing a holistic global regulatory i
 ntelligence program.\nAreas Covered in the Session :\nApplicable Laws 
 and Regulations\nDefinitions\nGuidance, Rules, and Standards\nWhat to 
 Consider for Regulatory Intelligence of Medical Products\nQuestions an
 d Issues to Identify and Address\nTotality and Flexible Approaches\nIn
 terfacing:  Roles and Benefits\nReimbursement and Intellectual Proper
 ty (IP) Issues\nAlignment between Regulatory Plan/Strategy, Reimbursem
 ent, and IP\nWhat to Integrate\nDetailed Contents\nCommon Mistakes Lea
 ding to Serious Consequences\nSpeaker’s PASS-IT Recommendations: Bes
 t Practices\nWho Will Benefit:\nCEOs\nVPs\nCompliance Officers\nAttorn
 eys\nRegulatory Affairs\nClinical Affairs\nQuality Assurance\nResearch
  & Development\nConsultants\nContractors/Subcontractors\nAnyone intere
 sted in Global Regulatory Intelligence Programs\n\nFor more informatio
 n visit https://medtechiq.ning.com/events/webinar-on-implementing-best
 -practices-for-global-regulatory
DTSTART;TZID=America/New_York:20160427T130000
DTEND;TZID=America/New_York:20160427T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=FDB1785
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=FDB1785
CONTACT:4169154458
ORGANIZER:Compliance Trainings
ATTACH;FMTTYPE="image/jpeg":
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=complianc
 etrainings:https://medtechiq.ning.com/profile/compliancetrainings
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