BEGIN:VCALENDAR VERSION:2.0 PRODID:-//ChamberMaster//Event Calendar 2.0//EN METHOD:PUBLISH X-PUBLISHED-TTL:P1H REFRESH-INTERVAL:P1H CALSCALE:GREGORIAN BEGIN:VTIMEZONE TZID:America/New_York BEGIN:DAYLIGHT RRULE:FREQ=YEARLY;BYMONTH=3;BYDAY=2SU DTSTART:20070101T000000 TZOFFSETFROM:-0500 TZOFFSETTO:-0400 TZNAME:Eastern Daylight Time END:DAYLIGHT BEGIN:STANDARD RRULE:FREQ=YEARLY;BYMONTH=11;BYDAY=1SU DTSTART:20070101T000000 TZOFFSETFROM:-0400 TZOFFSETTO:-0500 TZNAME:Eastern Standard Time END:STANDARD END:VTIMEZONE BEGIN:VEVENT DTSTART;TZID=America/New_York:20261104T083000 DTEND;TZID=America/New_York:20261104T160000 X-MICROSOFT-CDO-ALLDAYEVENT:FALSE SUMMARY:BSI Meet the Experts: In Vitro Diagnostic Regulation DESCRIPTION:About the event Navigating the path to bring an In Vitro Diagnostic to market starts by having the right information to comprehend the regulatory journey. Meet the Experts: IVDR will focus on understanding the requirements of the In Vitro Diagnostic Regulation (IVDR) and ISO 13485\, maintaining certification and managing post-market obligations. Whether you are an IVD manufacturer\, a regulatory affairs professional or an In Vitro Diagnostic (IVD) startup\, this event is your opportunity to gain insights and ask the questions that matter most. At the event\, you can expect to:Broaden your IVDR knowledge and understandingLearn what a successful IVDR submission looks likeUnderstand the pathway to CE markingGain knowledge of post-certification requirementsConnect directly with BSI's IVDR specialistsWhat will you gain?The latest updates on the IVDRReal-world case study and lessons learned from IVDR submissionsA live Ask the Experts Q&A sessionDeep-dive workshops to help you navigate the IVDRWho should attend?This event is designed for anyone navigating the IVDR regulatory landscape\, including:IVD manufacturers: new\, existing and transferring clientsStart-ups preparing for their first IVDR submissionRegulatory affairs and quality managersIVD consultantsRegister now and learn more BSI Meet the Experts: In Vitro Diagnostic Regulation X-ALT-DESC;FMTTYPE=text/html:

About the event \;

Navigating the path to bring an In Vitro Diagnostic to market starts by having the right information to comprehend the regulatory journey. Meet the Experts: IVDR will focus on understanding the requirements of the In Vitro Diagnostic Regulation (IVDR) and ISO 13485\, maintaining certification and managing post-market obligations. \;

Whether you are an IVD manufacturer\, a regulatory affairs professional or an In Vitro Diagnostic (IVD) startup\, this event is your opportunity to gain insights and ask the questions that matter most. At the event\, you can expect to:

Broaden your IVDR knowledge and understanding
Learn what a successful IVDR submission looks like
Understand the pathway to CE marking
Gain knowledge of post-certification requirements
Connect directly with BSI&rsquo\;s IVDR specialists

What will you gain?

The latest updates on the IVDR
Real-world case study and lessons learned from IVDR submissions
A live Ask the Experts Q&\;A session
Deep-dive workshops to help you navigate the IVDR

Who should attend?

This event is designed for anyone navigating the IVDR regulatory landscape\, including:

IVD manufacturers: new\, existing and transferring clients
Start-ups preparing for their first IVDR submission
Regulatory affairs and quality managers
IVD consultants

LOCATION:Boston MA 02451 UID:e.1244.1647985 SEQUENCE:3 DTSTAMP:20260930T114713Z URL:https://business.massmedic.com/events/Details/bsi-meet-the-experts-in-vitro-diagnostic-regulation-1939214?sourceTypeId=Hub END:VEVENT END:VCALENDAR