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Day 2 - Tuesday 16th June - CEST Time Zone
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Day 2 - Tuesday 16th June - CEST Time Zone
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Biocompatibility Workshop
09:00 - 09:40
Part 1: Opening Remarks & The State Of The Art In Biocompatibility
Gap analysis of existing biological evaluations under the new ISO 10993-1 revision
Workshop Summary: This interactive training will provide an overview of medical device biocompatibility with a focus on entire biological evaluation process from development of a biological evaluation plan through testing and biological evaluation report according to ISO 10993-1:2025 requirements
- Beau Rollins - Head of Biocompatibility, ConvaTec
09:40 - 10:20
Part 2: Structured Approach To Developing a Biological Evaluation Plan (BEP)
From regulatory intent to practical execution
- Marina Daineko - Biocompatibility Consultant, Intrinsic Medical Group
10:20 - 11:00
Part 3: Biological Risk Assessment in Practice
Risk identification, justification, and expectations
- Marina Daineko - Biocompatibility Consultant, Intrinsic Medical Group
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Biocompatibility Workshop
11:35 - 12:15
Part 4: Designing a Defensible Test Strategy Within The BEP
Aligning scientific rationale with ISO 10993 requirements
- Beau Rollins - Head of Biocompatibility, ConvaTec
12:15 - 12:45
Interactive Session: Activities 1 & 2
12:45 - 13:20
Part 5: Understanding and interpreting test results
Common pitfalls & resolution
- Beau Rollins - Head of Biocompatibility, ConvaTec
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Biocompatibility Workshop
14:35 - 15:15
Part 6: From BEP to BER: translating strategy into conclusions
Toxicological risk assessment (TRA), real-world examples and questions from agencies
- Marina Daineko - Biocompatibility Consultant, Intrinsic Medical Group
15:15 - 15:35
Practical Exercises: Activities 3 & 4
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Biocompatibility Workshop
15:55 - 16:35
Part 7: The life cycle of a biological evaluation
Change management, lifecycle updates & maintaining compliance
- Beau Rollins - Head of Biocompatibility, ConvaTec
16:35 - 16:55
Open Q&A + Expert Exchange
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