2nd Online Conference Biocompatibility Testing in Medical Devices

11th - 12th of May 2021, 15:00 CET

BigMarker platform

ABOUT THE CONFERENCE

We are pleased to welcome you to the 2nd Annual Biocompatibility Testing in Medical Devices Online
 Conference that will take place online on the 11 -12 of May, 2021 at 3:00 pm CET on BigMarker.

The 2nd Annual Biocompatibility Testing in Medical Devices Online Conference will give you
the unique opportunity to discuss the most pressing issues and meet the representatives of the biggest
companies and leaders from Biocompatibility and Medical Device Industries.

The 2nd Annual Biocompatibility Testing in Medical Devices Online Conference is a great platform for
learning, exchanging opinions, and expanding one’s network enabled by live presentations followed by
dynamic questions & answers sessions as well as panel discussions and workshops with keynote speakers. 

Key points

  • Latest updates on MD test irritation
  • Ways to comply with global regulatory changes
  • How to perform PMS under MDR
  • Direct and indirect body contact medical device
  • In Vitro Diagnostic Regulation
  • Remote Notified BodyAudits
  • How to comply with MHRA registration process
  • EU MDR upgrades explained

Who should attend

  • Consultants
  • Technical advisors
  • Product Managers
  • Laboratory Managers
  • System Engineers
  • Research Engineers
  • Design Engineers
  • Manufacturing Engineers
  • Quality Assurance Professionals
  • Regulatory Affairs Managers
  • R&D Engineers

Benefits of Attending 2 Annual Biocompatibility Testing in Medical Devices Online Conference:

  • 7+ different topics
  • panel discussion
  • networking with business professionals and industry experts
  • additional materials
If you would like to participate, kindly book your spot. The seats are limited.
Broadcast Link will be provided via email post registration.

Event Schedule

15:00 – 15:05 CET

Welcome and opening remarks from the Chairman

15:05 – 15:25 CET

2021 Updates on Test Irritation Caused by Medical Device: Key Factors of Result Interpretation + Q&A

15:25 – 15:50 CET

Ways to Simplify Compliance in Global Regulatory Changes + Q&A

15:50 – 16:00 CET

BREAK

16:00 – 16:25 CET

New Requirements of Material Characterization and Toxicological Risk Assessment for Medical Devices: Trends And Challenges + Q&A

16:25 – 17:50 CET

PANEL DISCUSSION: EU MDR Upgrades Explained

17:50 – 17:55 CET

CLOSING SESSION REMARKS

15:00 – 15:05 CET

Welcome and opening remarks from the Chairman

15:05 – 15:25 CET

Routes to Ensure a MDR Complaint PMS (Post-market Surveillance) System+ Q&A

15:25 – 15:50 CET

In Vitro Diagnostic Regulation Classification Issues+ Q&A

15:50 – 16:00 CET

BREAK

16:00 – 16:25 CET

How to Comply with MHRA Registration Process and Launch a Medical Device in UK+ Q&A

16:25 – 16:50 CET

Chemical Characterization of Medical Devices within a Risk Management+ Q&A

16:50 – 16:55 CET

CLOSING SESSION REMARKS

SPEAKERS

Galinyte Viktorija
Medical Device Specialist
NEOX Clinical Research Organization
Paolo Pescio
Business Unit Manager -Consulting
Eurofins Biolab
Alina Martirosyan
Scientific Manager Toxicology
B.Braun Melsungen
Mikolaj Krukowski
Medical Device Auditor
TUV SUD
Charlotte Elisabeth Laupheimer
Preclinical Research Manager & Medical Writer
Geistlich Pharma AG
Marta Carnielli
Technical Officer IVD
TÜV SÜD
Paul Malinovski
Director BU Consulting / Head of QM/RA
Pulmotree

Contact Us

Kara Koz
Conference Producer
Tel.: +420 228 227 163
E-mail: kara.koz@bcf-events.com
Valerie Neumann
Marketing Manager
Tel.: +420 228 227 162
E-mail: valerie.neumann@bcfgroup.eu
Benazir Jursunbek
Operations Manager
Tel.: +420 228 227 164
E-mail: operations@bcf-events.com