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2021 EUROPEAN MEDICAL DEVICE AND DIAGNOSTIC LABELLING & UDI VIRTUAL CONFERENCE


30TH NOVEMBER – 1ST 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 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

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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