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
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
Cyto and It's Challenges + Q&A
16:50 – 17:15 CET
PANEL DISCUSSION: EU MDR Upgrades Explained
17:15– 17:20 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
