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UID:2140535:Event:66801
DTSTAMP:20260902T073635Z
SUMMARY:Webinar On International product registrations – Lessons Lea
 rned?
DESCRIPTION:Description :\nThe focus of this session is international 
 product registration for IVDs & Medical Devices. Product registrations
  requirements have changed with new regulations across the globe. Requ
 irements have been clarified and in some cases the registration timefr
 ame has been reduced.\nIndustry Executives and investors are complaini
 ng these days that their competitive edge is being jeopardized by the 
 heightened regulatory scrutiny. For device companies based in the US, 
 there is a growing trend in commercializing their products outside the
  country. In particular, many US-based companies are targeting new mar
 kets in the EU, China and, increasingly, India.\nThe process for appro
 val or clearance of devices varies from regulatory body to regulatory 
 body. In some cases, products achieve regulatory approval in an effici
 ent and timely manner. In others, including the US FDA, companies may 
 face a protracted and delayed approval process. Recent scrutiny by US 
 regulators and legal authorities is making it more uncertain for compa
 nies attempting to gain market access in foreign countries.\nIn an eco
 nomy where getting the jump on your competitors is so important, this 
 training will provide a guide to ease international registrations and 
 reduce time to market. Learning the relevant regulatory requirements a
 nd the appropriate document legalization path will speed up the pathwa
 y.\nAreas Covered in the Session :\nInternational regulation- Overview
  of country by country differences\nRole and responsibilities of US ma
 nufacturers & in-country distributors\nIdentifying the key players\nWo
 rking with in-country distributors\nSales forecasting – Who needs to
  know?\nTypes of documents need\nMedical Device & IVDs\nBest practices
  for document legalizations\nApostille vs. Authentications\nHow to get
  documents embassy legalized\nPitfalls – What to look out for.\nWho 
 Will Benefit:\nRegulatory Affairs Specialists\nRegulatory Affairs Mana
 gers\nProduct Managers\nMarketing Professionals\nAdministrative Profes
 sionals\nTeams involved in new product registration\n\nFor more inform
 ation visit https://medtechiq.ning.com/events/webinar-on-international
 -product-registrations-lessons-learned
DTSTART;TZID=America/New_York:20151023T130000
DTEND;TZID=America/New_York:20151023T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=MD1643
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=MD1643
CONTACT:416-915-4458
ORGANIZER;CN=compliancetrainings:https://medtechiq.ning.com/profile/co
 mpliancetrainings
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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