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Submission: On October 28 via api from US — Scanned from GB
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Register to Attend Sponsor * Home * Agenda * Subscribe * Contact Us * Home * Agenda * Subscribe * Contact Us Open menu 2021 EUROPEAN MEDICAL DEVICE AND DIAGNOSTIC LABELLING & UDI VIRTUAL CONFERENCE 30TH NOVEMBER – 2ND DECEMBER 2021 | VIRTUAL EVENT DOWNLOAD THE 2021 AGENDAREGISTER TT DL, EUROPE’S ONLY CONFERENCE DEDICATED TO MEDTECH LABELLING AND UDI PROFESSIONALS WILL TAKE PLACE ON 30TH NOVEMBER, 1ST & 2ND DECEMBER 2021 Labelling received prominent attention in the MDR and IVDR regulations to ensure high standards of quality and safety of medical devices. The concept of including UDIs on the labels of medical devices is not new, the regulations also focused heavily on UDI and its importance to track a product. While most of the changes implemented by EU MDR and IVDR are very similar to the US FDA, the EU adopted stringent and tighter controls. The requirements laid out by the regulations are likely to result in labelling congestion. Failure to produce accurate, compliant labelling may result in organizations being unable to distribute their products in Europe, causing products to be unnecessarily stockpiled or even resulting in costly, product recalls. To ensure compliance with the regulation, it is critical to take small steps with the phased approach supported by the right technology to effectively implement the labelling and UDI processes. The 2021 European Medical Device and Diagnostic Labelling and UDI Virtual Conference is an interactive knowledge-sharing platform focused on developing effective and integrated strategies to further improve labelling and UDI processes and ensure compliance. Delving into the European medical device and diagnostic regulations, the three-day conference will unearth some of the best strategies for streamlining label approval operations and minimising human errors, the impact of EUDAMED delay, successful UDI application and implementation, and IFU content optimisation. Presentations supported with real-life case studies and practical examples will provide deeper insight into the strategies for labelling and UDI compliance. This conference will provide attendees an opportunity to participate in highly interactive sessions supported by real-life business examples, case studies, Q&A sessions, and round table discussions led by experienced professionals. First-hand experience and tips will be shared to enhance the end-to-end operational management of packaging and labelling for compliance with medical device and diagnostic regulations. Receive the actionable takeaways necessary to achieve your goals with innovative solutions for label development and delivery. IF YOU ARE A PART OF THE MEDTECH LABELLING, REGULATORY AND UDI COMMUNITY, TT DL GUARANTEES VALUABLE RETURN ON TIME INVESTED. 2021 TT DL SPEAKERS IVD TECHNICAL OFFICER TÜV SÜD PRODUCT SERVICE GMBH DIRECTOR, UDI & MASTER DATA MANAGEMENT MASIMO SENIOR MANAGER HEALTHCARE GS1 GLOBAL MEDICAL DEVICES CERTIFICATION MANAGER SGS REGULATORY AFFAIRS LABELING SPECIALIST ALCON ENGAGEMENT MANAGER GS1 MANAGER, GLOBAL LABELLING SYSTEMS ARTHREX GLOBAL MASTER DATA SYNCHRONIZATION LEADER - PROJECT LEADER MASTER DATA FOR EUROPEAN UDI COMPLIANCE BIOMERIEUX GLOBAL UDI PROGRAM MANAGER FOR WOUND SMITH & NEPHEW PARTNER HOGAN LOVELLS INTERNATIONAL LLP REGULATORY AFFAIRS MANAGER BHS TECHNOLOGIES GLOBAL SENIOR LEADER FOR MEDICAL DEVICE, COMBINATION PRODUCT AND PHARMACEUTICAL ORGANIZATIONS MALLINCKRODT PHARMACEUTICALS REGULATORY AFFAIRS MANAGER (IVDR, SOFTWARE, PMS) OXFORD NANOPORE TECHNOLOGIES LTD GLOBAL PROJECT MANAGER UDI SYSTEMS ZIMMER BIOMET QUALITY ASSURANCE LEADER CYTIVA LABELLING & ARTWORK CROMA-PHARMA LABELLING MANAGER, GLOBAL LABELLING ZIMMER BIOMET MANAGER REGULATORY AFFAIRS - TEAM LEAD DIABETES CARE YPSOMED AG Register Your PositionRegister A GroupRegister to SpeakSponsorBook a Hotel Room FEATURING -------------------------------------------------------------------------------- 80+ MedTech Labelling, Regulatory and UDI professionals 20+ Solution-Focused Topics 7 Hours of Networking TESTIMONIALS WHAT OUR ATTENDEES HAVE SAID Regulatory Affairs / Medical Device Safety OfficerOCCLUTECH GMBH Satisfied with the conference because of possibility to talk to the experts, to ask specific questions and have good conversations. Post Market Surveillance International – Senior AnalystHOLOGIC N.V. Interesting presentations related to the upcoming challenges for the new EU MDR. Co-Founder, CTO & InnovationMOVENDO TECHNOLOGY S.r.l I enjoyed the meeting very much. The quality of the peers and the talks was very high and had some very inspiring speeches. Senior Manager, Quality Regulatory & Compliance EMEAORTHO CLINICAL DIAGNOSTICS Very good presentations, excellent exchanges with participants, good logistics. Global Director – Cardiovascular Focus TeamTÜV SÜD PRODUCT SERVICE I found the meeting interesting and from my perspective the interaction with the other attendees has been very fruitful. Sr. Certification OfficerNSAI Great people and great event. I really enjoyed it. Valuable use of time. Senior Design Assurance ManagerVERYAN MEDICAL LTD A wonderful opportunity to meet experienced, skilled and open-minded people willing to share solutions in this ever-changing medical device environment. Head - Corporate Quality Management & Quality ComplianceINSTITUT STRAUMANN AG Good presentations and interactions. Interesting exchange with other participants. Regulatory Affairs / Medical Device Safety OfficerOCCLUTECH GMBH Satisfied with the conference because of possibility to talk to the experts, to ask specific questions and have good conversations. Post Market Surveillance International – Senior AnalystHOLOGIC N.V. Interesting presentations related to the upcoming challenges for the new EU MDR. Co-Founder, CTO & InnovationMOVENDO TECHNOLOGY S.r.l I enjoyed the meeting very much. The quality of the peers and the talks was very high and had some very inspiring speeches. Senior Manager, Quality Regulatory & Compliance EMEAORTHO CLINICAL DIAGNOSTICS Very good presentations, excellent exchanges with participants, good logistics. Global Director – Cardiovascular Focus TeamTÜV SÜD PRODUCT SERVICE I found the meeting interesting and from my perspective the interaction with the other attendees has been very fruitful. Sr. Certification OfficerNSAI Great people and great event. I really enjoyed it. Valuable use of time. Senior Design Assurance ManagerVERYAN MEDICAL LTD A wonderful opportunity to meet experienced, skilled and open-minded people willing to share solutions in this ever-changing medical device environment. Head - Corporate Quality Management & Quality ComplianceINSTITUT STRAUMANN AG Good presentations and interactions. Interesting exchange with other participants. ‹› WHY ATTEND TT DL LIVE INTERACTIVE CONTENT TT DL is a collaborative environment for learning with a powerful mix of interactive content. With breakout sessions and an informal Q&A after every session; panel debates, case studies and workshops; TT DL delivers all labelling and UDI strategy content you need in the most engaging format. MEET YOUR COUNTERPARTS With one of the most robust screening processes in the industry, all attendees will be in an environment full of MedTech Labelling, Regulatory and UDI experts, exclusively. Attendees can ask their most important questions to the group for direct replies from elite industry experts. CUSTOMISE YOUR CONTENT TT’s DL will allow attendees to pick the subjects most relevant to them. This tailored event experience ensures each attendee receives the information, and networking opportunities, most applicable to their day-to-day role. CONTACT UK Tel: +44 (0)1753 336 041 Email: info@ttgw.co.uk Fifth Floor The Atrium 1 Harefield Road Uxbridge UB8 1EX CONTACT ASIA Tel: +44 (0)1753 336 041 Email: info@ttgw.co.uk A-206, 2nd Floor Crystal Plaza, New Link Road Andheri West, Mumbai India