Kymanox

Life Science Solutions

Science EN ↓ 46 episodes

Presented by Kymanox, Life Science Solutions is dedicated to accelerating understanding and advancing expertise in the life sciences industry. Focused on bringing industry insights to light, our podcast offers a platform where regulatory, scientific, and engineering experts share practical knowledge on overcoming the challenges of product development and commercialization. Episodes equip listeners with the latest on regulatory updates, market trends, cutting-edge technology, and more. Join us as we explore the journey of modern medicines, ensuring every product reaches its full potential in sa...

Author

Kymanox

Category

Science

Podcast website

www.kymanox.com

Latest episode

Jun 23, 2026

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Episodes

Aligning with the Right CMO 13.05.2024

Today's episode is all about Contract Manufacturing Organization (CMO) selection. When organizations are considering a CMO, how do they find the right one for them? We're joined by two Kymanox executives, Ryan Doxey, Senior Director of Technical Services, and Jason Martin, Senior Director of CGXP Technical Services. They highlight the importance of finding a CMO with the right capabilities and exp...

Mastering the Product Development Lifecycle for Commercial Readiness 15.04.2024

How can medical device and combination product companies bridge the difficult "valley of death" between early product design and commercial readiness?  In this episode, Nick Ciccarelli, Chief Technology Officer at Kymanox, shares insights into their integrated product design, development, and commercialization approach with host Evan Edwards, Chief Innovation Officer. He explains how their cross-f...

QMSR, ISO 13485:2016, and What It All Means for Medical Device Risk Management 18.03.2024

Naveen Agarwal, PhD and Nate Blazei discuss the QMSR and the relationship to ISO 13485:2016 and how Risk Management is the cornerstone to success.  The new Quality Management System Regulation (QMSR) from the FDA represents a significant shift in expectations for how medical device companies manage their quality systems. At its core, QMSR requires companies to take a more process-based and risk-ba...

Kymanox: Two Decades of Excellence 15.02.2024

Take a trip to 2004 for a moment. Yahoo was the #1 website on the planet. Mark Zuckerberg came up with Facebook. 14-year-old Taylor Swift signed on with Sony to pursue her career in country music.   And from Stephen and Sarah Perry's perspectives, the Life Science industry was in desperate need of improvement. There was a lot of bureaucracy and red tape, and modern medicine that needed to be in pa...

The Path to Sustainable Practices in Medical Device Design and Combination Product Manufacturing 09.01.2024

Sustainability isn’t a buzzword - it’s a crucial aspect of the mission within medical device and combination product design and manufacturing. But it’s not always easy to figure out all the design considerations that make products cost efficient, sanitary, AND sustainable.  So how can we do it as an industry? Today, Cormac O’Prey, Principal and Director at the Kestrel Consultancy Group , and Agili...

AI Summit Highlights: Transparency, Bias in AI, and Exciting Advances 18.12.2023

The Agilis by Kymanox experts in digital health, Lauren Horn, PhD and Alexandria Kruzer, attended the 2023 AI Summit and share their key takeaways. They showcased a notable shift in AI discussions from continuous learning to the evaluation of large language learning models. Transparency in AI, particularly using SHAP values, emerged as a critical theme, contributing to the usability of algorithms....

Innovating Patient-Centric Healthcare: A Conversation with Stephen M. Perry 06.12.2023

In the conclusion of our conversation with Stephen M. Perry ( part 1 ) we explore the dynamic intersection of healthcare innovation and patient-centered solutions. Exploring the evolution from traditional clinic-based treatments to innovative home-based therapies, they highlight the impact on patient experiences, emphasizing dignity, reduced anxiety, and improved quality of life. Discover how Kyma...

Combination Product Universe: PDA Conference Recap with Keynote Speaker Stephen Perry 20.11.2023

At the PDA Universe of Pre-filled Syringes and Injection Device Conference in Gothenburg, Sweden, Kymanox Founder and CEO Stephen Perry delivered a keynote address titled "The Inspiring Evolution of Parenteral Combination Products from 2004 to Today from an Entrepreneurial Perspective – And a Peek at What Is Coming."   Stephen Perry provides a comprehensive overview of the historical evolution of...

Unpacking the Role of Human Factors in Medical Device Development 08.11.2023

Shannon Hoste and Rita Lin discuss Rita's recent presentation at the RAPS Convergence conference in Montreal and share insights about their experiences in the field of human factors and regulatory affairs in the medical device industry. They touch on various topics, including the challenges and opportunities in combination product development, the importance of risk management, regulatory consider...

Navigating the Real-World Environment of Medical Products 25.10.2023

In this episode, Rita Lin and Shannon Hoste share their experiences and journeys in the field of human factors engineering. Rita begins by recounting her path into healthcare, describing how she ventured into remote areas to provide support with donated medical devices. This eye-opening experience underscored the critical importance of considering usability and human factors in product design. Sha...

Creating a Successful Roadmap: Lab, Clinic, Market 11.10.2023

In this episode of The Factor, Shannon continues her conversation with Stefanie Johns, PhD, Director of Regulatory Affairs at Kymanox ( part 1 ). They review how companies can a create a successful roadmap to bring their product from lab to clinic and commercialization. Reviewing the importance in understanding the therapeutic index, understanding users, how best to manage risk, and incorporating...

Factors to Consider in Clinical Readiness for Medical Device and Combination Product 25.09.2023

How do you know your combination product is ready for clinical trials? Will it pass the regulatory review for clinical approval to proceed? The complexities of harmonizing drug and device elements, managing risks, and understanding variability can be overwhelming. If clinical readiness is on your product development plan, join our discussion with Dr. Stefanie Johns, Director of Regulatory Affairs...

Future Healthcare Models: The Evolving Role of Nurses in Advancing Patient-Centered Care 13.09.2023

Dr. Bonnie Clipper , the founder of Innovation Advantage , a consultancy specializing in helping healthcare organizations embrace innovation, discusses various aspects of healthcare models, technology impact and the evolving role of nurses. Dr. Clipper highlights the importance of incorporating technology, such as virtual reality, into training healthcare professionals and utilizing assistive tech...

Transforming Nursing through AI and Innovation, with Dr. Bonnie Clipper 29.08.2023

Today we explore the dynamic synergy between healthcare innovation and human factors engineering in nursing, with Dr. Bonnie Clipper . We focus on patient care transformation through bridging the technology gap, standardizing practices, and optimizing medical device integration. This episode will emphasis the need for collaboration between medical device manufacturers, health care institutions, an...

Navigating the Challenges of UDI Compliance in Europe's Evolving Regulatory Landscape (Part 2 with Dr. Christiana Hofmann and Richard Houlihan) 16.08.2023

In this episode of The Factor Podcast, industry experts Dr. Christiana Hofmann and Richard Houlihan discuss the complexities of Unique Device Identification (UDI) compliance in the evolving European regulatory landscape. From the daunting task of collating data to the importance of strategic planning, they reveal the critical factors that can make or break a successful UDI implementation. Join the...

Exploring EUDAMED Requirements for EU MDR, with Richard Houlihan and Christiana Hofmann 02.08.2023

In this informative episode of The Factor, we sit down with industry experts Dr. Christiana Hofmann and Richard Houlihan to discuss critical aspects of EUDAMED, the European Union's Medical Device Database, and the EU MDR's implementation journey. The creation of a European database on medical devices (EUDAMED) is one of the key aspects of the new rules on medical devices (Regulation (EU) 2017/745...

(Part 2) Winning Formula: Combination Products Unveiled, with Susan Neadle 19.07.2023

Today, Susan Neadle and Stephanie Canfield are back for part two. If you haven't listened to part one , do that first and then come back to this episode. Susan and Stephanie chatted about Susan's new book, The Combination Products Handbook : A Practical Guide for Combination Products and Other Combined Use Systems. And how it brings clarity of understanding for global Combination Products guidance...

Winning Formula: Combination Products Unveiled, with Susan Neadle 05.07.2023

Susan Neadle recently penned the highly anticipated " Combination Products Handbook ," a practical guide that distills her years of industry experience into a comprehensive resource. She shares the backstory behind the book and its journey to becoming a peer-reviewed publication by the FDA. With Stephanie Canfield and Shannon Hoste, they discuss the top considerations in Combination Products, cove...

(Part 2) ISO 14971 and Risks in Medical Devices: What You Need to Know 21.06.2023

In part one , we chatted about the overarching risk management process for medical device development. Today we continue the conversation, digging into the complexities of medical devices, including AI and other MedTech. Can risk management keep up with the evolving medical tech landscape? What about complex systems? Let's find out. Today's episode is hosted by Denise Wagner, Senior Director of Hu...

Risk Management, Innovation and Safety in Medical Devices: Evolving from Compliance to Excellence 08.06.2023

Today we discuss the current developments and trends surrounding risk management in the medical device industry. Our guests are Edwin Bills and Shannon Hoste, and they touch upon the challenge of consolidating numerous standards and documents while ensuring the consideration of overall residual risk, encompassing aspects like AI, cybersecurity, and biocompatibility.  The conversation explores the...

Secret to Succes: Human Factors for Medical Product Development 05.12.2022

EP1: Human Factors Secrets to Success.  In this episode the host, Sophia Kalita, interviews Pat Patterson and Shannon Hoste with Agilis Consulting Group on how they found themselves drawn to MedTech and what they hope to continue to accomplish.     Memorable Quotes:   If you understand the importance of being able to describe human performance and are, are able to do that to me that's the secret s...

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