We are excited to host a guest speaker, an expert in medical device process development, whose extensive experience spans across industry and research. This podcast offers a deep dive into the journey of taking a medical device from concept to manufacturing, the challenges of regulatory compliance, the impact of automation, and insights into working in this dynamic field. Whether you're a seasoned professional or new to the medical device industry, this discussion promises to provide valuable perspectives and practical advice.

Timeline:

01:50 Guest self-introduction

02:55 The experience that shaped their experiment skill sets

05:10 First industry experience

07:00 Maintaining a positive attitude during massive layoffs

08:00 Passion for diagnostic tools

11:30 Day-to-day work life, from concept to product manufacturing

● discussion of the development pipeline:

concept -- prototype -- process (scale up)

● Importance of finalizing processes during development since changes are restricted post-manufacturing due to regulatory requirements.

16:35 Biosensor technologies and current research status

20:20 Medical device classification and regulatory overview

● Classification based on device risk levels

Class II Medical Device Regulation:

ISO 10993: Framework for biocompatibility evaluation.

ISO 14971: Risk management for medical devices.

ISO 13485: Quality management system for manufacturing.

24:00 Premarket Approval (PMA) submission

24:40 Premarket Notification (510(k)) process

27:15 Clinical trial requirement for medical device (feasibility study/ pivotal trial)

29:00 Detailed explanation of ISO 10993

31:40 Clean room costs

34:35 Importance of clean room and sterilization process

38:25 Handling contamination from machines

40:15 Impact of automation in the medical device industry

42:20 Process that can not be automated

45:00 Challenges in implementing automatio

47:38 The future of automation

48:20 Challenges in Medical Device Process Development

50:50 Industry vs. research

52:52 Large company vs. start-ups

56:45 Advice for aspiring medical device professionals

59:15 Case study

Glossary:

Feasibility Study: An early-stage clinical trial designed to evaluate the safety and preliminary efficacy of a medical device.

ISO 10993: An international standard for assessing the biocompatibility of medical devices.

ISO 13485: An internationally recognized standard for a quality management system (QMS) for medical device manufacturing.

ISO 14971: A standard outlining risk management processes for medical devices.

Premarket Approval (PMA): The FDA’s regulatory pathway for Class III devices, requires robust evidence of safety and effectiveness.

Premarket Notification (510(k)): A less stringent FDA pathway for demonstrating that a new device is substantially equivalent to a legally marketed device (predicate).

Prototype: An early working version of a medical device used for testing and refinement during development.

Quality Management System (QMS): A structured system of procedures and processes ensuring that medical devices meet regulatory and quality standards.

Risk Management (ISO 14971): The systematic application of policies, procedures, and practices for identifying, evaluating, and controlling risks associated with medical devices.

Navigating Medical Device Development

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