UPCOMING WEBINAR
Bridging Design & Manufacturing In Medtech: THE DFM APPROACH
WHAT IS IT ALL ABOUT ?
Design for Manufacturability (DFM) plays a crucial role in the success of medical devices, impacting cost, quality, scalability, and regulatory compliance. Poor design decisions can lead to costly redesigns, production inefficiencies, and regulatory hurdles.
This webinar, hosted by IZiel Healthcare, will provide actionable insights on integrating DFM principles into medical device development. Atul Mahajan, Director, Engineering Services at IZiel, will share industry best practices and strategies to ensure a smooth transition from design to manufacturing.
SPEAKERS AND TOPICS
Topics Covered
- Importance of DFM in Medical Device Development
- Strategies to Reduce Manufacturing Costs Without Compromising Quality
- Material Selection for Biocompatibility and Regulatory Compliance
- Optimizing Tolerances and Design for Assembly (DFA)
- Aligning Designs with FDA, EU MDR, and ISO 13485 Requirements
- Common Pitfalls and How to Avoid Costly Redesigns
Topics Covered
- Importance of DFM in Medical Device Development
- Strategies to Reduce Manufacturing Costs Without Compromising Quality
- Material Selection for Biocompatibility and Regulatory Compliance
- Optimizing Tolerances and Design for Assembly (DFA)
- Aligning Designs with FDA, EU MDR, and ISO 13485 Requirements
- Common Pitfalls and How to Avoid Costly Redesigns
Sarvesh Mutha
Managing Director
Click here to schedule a call
Topics Covered
- Importance of DFM in Medical Device Development
- Strategies to Reduce Manufacturing Costs Without Compromising Quality
- Material Selection for Biocompatibility and Regulatory Compliance
- Optimizing Tolerances and Design for Assembly (DFA)
- Aligning Designs with FDA, EU MDR, and ISO 13485 Requirements
- Common Pitfalls and How to Avoid Costly Redesigns
Sarvesh Mutha
Managing Director
Click here to schedule a call
GALLERY
Preview of the Seminar conducted by IZiel along with their partners.
This Webinar is conducted by IZiel
