Advertise on podcast: Gradical Podcast - The Podcast about Plastics in Medical Technology

"Is this material going to be biocompatible?" is one of the most commonly asked questions in medical device development. The problem is, there's no such thing as a biocompatible material. In this episode, I speak with Marina Daineko, Biocompatibility Consultant at Intrinsic Medical Group, about how biological risk assessment actually works, what mistakes companies make early in development, and how to incorporate biocompatibility thinking during prototyping without running full testing on every grade. This conversation is technical, practical, and based on real consulting work. We talk about the ISO 10993-1 framework, extractables and leachables, CMR substances, and why a structured plastic selection process helps you mitigate biological risk before it becomes a costly problem. If you work in MedTech and want to understand how to think about biocompatibility earlier in development, this episode will help you make better material decisions and avoid expensive surprises late in the process. 🔗 CONNECT WITH MARINA DAINEKO:  Intrinsic Medical Group: https://www.intrinsicmedicalgroup.com/ LinkedIn: https://www.linkedin.com/in/marinadaineko/ Connect with us:  🎧 Subscribe to the Gradical Podcast for insights on MedTech materials and innovation  🟣 Apple Podcasts – https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554  🟢 Spotify – https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq  📺 YouTube – https://www.youtube.com/@GradicalGmbH  🌍 Learn more about Gradical: https://gradical.ch/  📩 Work with Lucas and the team: [email protected] #GradicalPodcast #MedTech #MedicalDevices #Sustainability #Biocompatibility #Plastics #ISO10993 #MaterialSelection Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Chemical recycling is often presented as a silver bullet. But is it actually viable for medical-grade plastics? In this episode, I speak with Reinier Grimbergen, CTO of Blue Circle Olefins, about what chemical recycling really is, how it differs from mechanical recycling, and where it actually makes sense for MedTech. This conversation is technical, practical, and grounded in industrial reality. We talk about pyrolysis vs gasification, energy trade-offs, feedstock constraints, economics, and why some recycling routes can deliver virgin-quality polymers suitable for medical and food-contact applications. Inside this episode, you will learn: ✔ What chemical recycling actually means at the molecular level ✔ Why mechanical recycling alone likely caps out around 40 percent ✔ Why higher energy use can enable higher-quality recycled polymers ✔ How chemical recycling could unlock circular plastics for medical applications ✔ What determines the economics of chemical recycling at scale If you work in MedTech and want to understand where chemical recycling actually fits, this episode will help you think more clearly about materials, sustainability claims, and long-term feasibility. 🔗 Connect with Reinier Grimbergen: Blue Circle Olefins: https://bluecircle-olefins.com/ LinkedIn: https://www.linkedin.com/in/reiniergrimbergen/ Connect with us: 🎧 Subscribe to the Gradical Podcast for insights on MedTech sustainability and innovation 🟣 Apple Podcasts – https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554 🟢 Spotify – https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq 📺 YouTube – https://www.youtube.com/@GradicalGmbH 🌍 Learn more about Gradical: https://gradical.ch/ 📩 Work with Lucas and the team: [email protected] If you're a MedTech company struggling to make your devices more sustainable, CLICK here: https://lucaspianegonda.clickfunnels.com/optin1756907952105 Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Why does it take so long to bring a medical device to market? And what can we actually do about it? Spencer Jones is a serial entrepreneur and the founder of XO MedTech and MedTech Vendors. In this episode, he breaks down the real problems slowing innovation in medical technology and shares practical solutions that work. This isn't about motivation. It's about the structural issues that make MedTech innovation slow, expensive, and isolating—and the systems that can fix them. Inside this episode, you will learn: ✔ Why clinical innovators struggle to translate their ideas into manufacturable devices  ✔ How the "glue person" who connects clinical needs to engineering is rare and critical  ✔ Why most innovators should try to get their competitors to steal their ideas (seriously)  ✔ How lean development and rapid customer feedback prevent year-long mistakes  ✔ Why engineers should see surgical cases and clinicians should visit manufacturing facilities ✔ Where AI can save massive time in MedTech (hint: it's documentation)  ✔ Why most MedTech teams need better vendor selection frameworks Spencer shares real examples from his experience taking devices from idea through FDA clearance, raising $10M in venture capital, and working across vascular access, laparoscopic surgery, and orthopedic devices. If you want to move faster, work smarter, and stop burning time on preventable mistakes, this conversation will help. If you're a MedTech company struggling to make your devices more sustainable, CLICK here: https://lucaspianegonda.clickfunnels.com/optin1756907952105 Connect with Spencer Jones: XO MedTech: https://xomedtech.com/ LinkedIn: https://www.linkedin.com/in/medtech-innovation/ Connect with us: 🎧 Subscribe to the Gradical Podcast for insights on MedTech sustainability and innovation 🟣 Apple Podcasts – https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554 🟢 Spotify – https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq 📺 YouTube – https://www.youtube.com/@GradicalGmbH 🌍 Learn more about Gradical: https://gradical.ch/ 📩 Work with Lucas and the team: [email protected] Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

If you are building or scaling a medical device, sterilization problems will catch up with you. Usually later in the process than you want. In this episode, I speak with Manuel Grandy, Consultant and Managing Partner at SteriComp GmbH, about what sterilization actually means in practice and why so many teams underestimate it until regulators start asking uncomfortable questions. We talk about ETO gas, gamma radiation, and why there is no universally “correct” sterilization method. The right choice depends on materials, device design, supply chain constraints, and how well you understand the science behind the standards. Manuel explains why sterile does not mean clean, why following a standard word-for-word is sometimes not enough, and how small decisions like where you place a biological indicator can delay approval by months. If you work in MedTech development, quality, regulatory, or manufacturing, this episode will help you avoid painful surprises and make better decisions much earlier. Connect with Manuel Grandy: LinkedIn: https://www.linkedin.com/in/sterilisation/ Connect with us: 🎧 Subscribe to the Gradical Podcast for insights on MedTech sustainability and innovation 🟣 Apple Podcasts – https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554 🟢 Spotify – https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq 📺 YouTube – https://www.youtube.com/@GradicalGmbH 🌍 Learn more about Gradical: https://gradical.ch/ 📩 Work with Lucas and the team: [email protected] #GradicalPodcast #MedTech #MedicalDevices #Sustainability Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Many companies say sustainability matters, but only a few treat it as part of their strategy. One of them is Ambu, a global MedTech company and the market leader in single-use endoscopy. In this episode, Casper Venbjerg Hansen, Senior Director, Sustainability, Public Affairs, Risk and Compliance at Ambu A/S, explains how sustainability guides their decisions and why Ambu committed to it early. Casper walks through Ambu’s long history with sustainability, including why they redesigned their endoscopes in 2009 to make future recycling possible. He shares how sustainability became strategic in 2022 when hospitals began asking for better environmental performance. We talk about single-use and reusable systems, the real footprint of reprocessing, and why raw materials drive a large part of emissions. Casper also explains how Ambu introduced bioplastics across all endoscope categories, how their takeback and recycling program works, and what it means to design for circularity from the start. If you want a practical look at how sustainability becomes a business advantage, this episode gives you a clear introduction. Connect with Casper Venbjerg Hansen: LinkedIn: https://www.linkedin.com/in/casper-venbjerg-hansen-322853/ Connect with us: 🎧 Subscribe to the Gradical Podcast for insights on MedTech sustainability and innovation 🟣 Apple Podcasts – https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554 🟢 Spotify – https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq 📺 YouTube – https://www.youtube.com/@GradicalGmbH 🌍 Learn more about Gradical: https://gradical.ch/ 📩 Work with Lucas and the team: [email protected]  #GradicalPodcast #MedTech #MedicalDevices #Sustainability Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Many organizations rely on LCAs (Life Cycle Assessments) to guide sustainability decisions, but the method is only as reliable as the data and assumptions used to build it. In this episode, Thomas Kägi, Member of the Board at Carbotech AG, explains how to structure an LCA so that the results reflect real environmental impact and not just guesses or incomplete boundaries. Thomas describes how the functional unit sets the entire frame for an analysis, why the use phase can overshadow production in environmental impact, and how to work with supplier-specific data when it is available. He also breaks down when uncertainty matters, how to start with a screening LCA, and why rules such as ISO standards and EPDs are essential for making comparisons that are fair. In this conversation, we cover: Why an LCA only makes sense when the underlying question is clearHow system boundaries shape the outcome of a studyWhy the use phase can account for most of a product's impactHow to work with databases and supplier-specific dataWhen uncertainty in LCA data matters and when it does notHow standards create comparability across different products🎧 If you want a practical understanding of how environmental impact is measured and how to avoid common mistakes, this episode provides a grounded and straightforward guide. Connect with Thomas Kägi: LinkedIn: https://www.linkedin.com/in/thomas-k%C3%A4gi-262648a0/ Connect with us: If you're a MedTech company evaluating commercialization risk or sustainability challenges, let’s talk: https://lucaspianegonda.clickfunnels.com/optin1756907952105 🎧 Subscribe to the Gradical Podcast for insights on MedTech sustainability and innovation: 🟣 Apple Podcasts – https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554 🟢 Spotify – https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq 📺 YouTube – https://www.youtube.com/@GradicalGmbH 🌍 Learn more about Gradical: https://gradical.ch/ 📩 Work with Lucas and the team: [email protected] Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Hospitals review new devices through a process that is far more complex than most teams expect. In this episode, commercialization specialist Jim Surek explains how he evaluates medical technologies and the three-part funnel he uses to predict whether a product will find traction. Jim describes how clinical performance, economic outcomes, and strategic or operational effects shape hospital decisions and why progress in only one area is not enough. In this conversation, we cover: Why clinical gains must connect to measurable economic valueHow Jim structures a commercialization assessmentHow hospitals view workflow changes and resource requirementsHow reimbursement shapes the path from prototype to adoptionWhat separates market-changing ideas from incremental improvements🎧 If you want to understand how hospitals make purchasing decisions and how to position your device for success, this episode is a focused and practical guide. Connect with Jim Surek: LinkedIn: https://www.linkedin.com/in/jimsurek Connect with us: If you're a MedTech company evaluating commercialization risk or sustainability challenges, let’s talk: https://lucaspianegonda.clickfunnels.com/optin1756907952105 🎧 Subscribe to the Gradical Podcast for insights on MedTech sustainability and innovation: 🟣 Apple Podcasts – https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554 🟢 Spotify – https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq 📺 YouTube – https://www.youtube.com/@GradicalGmbH 🌍 Learn more about Gradical: https://gradical.ch/ 📩 Work with Lucas and the team: [email protected] #GradicalPodcast #Sustainability #MedTech #MedicalDevices Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Every MedTech company wants to innovate faster, but most are slowed down by one thing they barely realize is consuming half their development time: technical documentation. In this episode, Karl J. Larsson, co-founder of Aligned, explains how Word- and Excel-based documentation structures create massive inefficiencies, audit delays, and innovation bottlenecks, and how a lean, software-driven approach transforms both speed and confidence. In this conversation, Karl and Lucas discuss: Why up to 50% of product development time is spent on documentationHow inconsistent files create “audit anxiety” and costly review cyclesThe real impact of moving from documents to design controlsHow automation strengthens change control and accelerates market access Why freeing engineers from paperwork fuels innovation and sustainability🎧 If you’re tired of documentation slowing your R&D team down, this episode is your roadmap. Connect with Karl J. Larsson: Website: https://www.aligned.ch LinkedIn: https://www.linkedin.com/in/karl-johan-larsson-bab4312/ Connect with us: If you’re a MedTech company struggling with documentation or sustainability challenges, let’s talk: https://lucaspianegonda.clickfunnels.com/optin1756907952105 🎧 Subscribe to the Gradical Podcast for insights on MedTech sustainability, materials, and innovation: 🟣 Apple Podcasts – https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554 🟢 Spotify – https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq 📺 YouTube – https://www.youtube.com/@GradicalGmbH 🌍 Learn more about Gradical: https://gradical.ch/ #GradicalPodcast #Sustainability #MedTech #MedicalDevices Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Marcel Kunz, Head of Packaging at Straumann Group, has spent his career making dental implant packaging safe, sterile, and sustainable. In this episode, he joins Lucas Pianegonda to share Straumann’s six “Golden Rules” for designing medical packaging that balances compliance with circularity — plus the story behind his toothbrush project that turned blister waste into a useful consumer product. They cover: The real cost of sterile barrier systems in MedTech Why Straumann won’t wait until 2034 to adapt to PPWR How a recycling experiment became a proof of concept for innovation How sustainability connects patient safety with long-term impactIf you work in medical packaging or device design, this episode will change how you think about “waste.” Connect with Marcel: https://ch.linkedin.com/in/marcel-kunz-4250b373 Connect with Straumann: https://www.straumann.com/group/us/en/home.html Connect with us: If you’re a medtech company struggling to make your devices more sustainable, let’s talk: https://lucaspianegonda.clickfunnels.com/optin1756907952105 🎧 Subscribe to the Gradical Podcast for insights on MedTech sustainability, materials, and innovation: 🟣Apple Podcasts https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554  🟢Spotify https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq 📺Watch these episodes on YouTube: https://www.youtube.com/@GradicalGmbH 🌍 Learn more about Gradical: https://gradical.ch/ 📩 Work with Lucas and the team: [email protected] #GradicalPodcast #Sustainability #MedTech #MedicalDevices Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

When Thomas Willemsen became CEO of GaleMed Group, he saw an opportunity to redefine medical consumables for a sustainable future. In partnership with Gradical, his team created the BioVent-Circuit — the world’s first anesthesia and ventilation circuit made from sugarcane-based bioplastic. In this conversation, Thomas and Lucas Pianegonda discuss:  • How GaleMed turned a concept into a validated, high-performing product  • Why sustainability is a strategic advantage, not a cost burden  • The challenges of market adoption in Europe and the U.S.  • How Gradical helped bridge regulatory and materials expertise  • What it takes to build category leadership in eco-consumables 📍 See the BioVent-Circuit at the GaleMed booth Hall 11/C51 during the Medica Fair in Düsseldorf, starting November 17 Connect with Thomas Willemsen: LinkedIn: https://tw.linkedin.com/in/thomas-willemsen-32696b21 Connect with GaleMed: https://www.galemed.com/en Connect with us: If you’re a medtech company struggling to make your devices more sustainable, let’s talk: https://lucaspianegonda.clickfunnels.com/optin1756907952105 🎧 Subscribe to the Gradical Podcast for insights on MedTech sustainability, materials, and innovation: 🟣Apple Podcasts https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554  🟢Spotify https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq 📺Watch these episodes on YouTube: https://www.youtube.com/@GradicalGmbH 🌍 Learn more about Gradical: https://gradical.ch/ 📩 Work with Lucas and the team: [email protected] #GradicalPodcast #Sustainability #MedTech #MedicalDevices Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Industrial design engineer Pablo Yániz González, who recently graduated in Integrated Product Design at TU Delft's Faculty of Industrial Design Engineering, set out to make a single-use inflator more sustainable and ended up designing a hybrid device that can be reused up to 1,000 times. In this episode, Pablo joins Lucas Pianegonda to discuss how hospitals can reduce waste without adding burden for clinicians, what “hybrid-use” design really means, and how to navigate the long, expensive road from prototype to regulatory approval. They cover: The tradeoffs between reuse and remanufacturing in hospitalsDesigning inflators that maintain safety and simplicityThe “Tesla lesson” for medtechWhy getting from prototype to MDR approval is a 3-year journey before sales even beginIf you’re an engineer or medtech innovator thinking about sustainability, this episode is for you. Connect with Pablo: LinkedIn: https://www.linkedin.com/in/pablo-yaniz-gonzalez Connect with us: If you’re a medtech company struggling to make your devices more sustainable, let’s talk: https://lucaspianegonda.clickfunnels.com/optin1756907952105 🎧 Subscribe to the Gradical Podcast for insights on MedTech sustainability, materials, and innovation: 🟣 Apple Podcasts – https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554 🟢 Spotify – https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq 📺 YouTube – https://www.youtube.com/@GradicalGmbH 🌍 Learn more about Gradical: https://gradical.ch/ 📩 Work with Lucas and the team: [email protected] Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Dr. Axel Boese has spent years studying how hospitals can innovate sustainably — and one of his biggest insights challenges the status quo of “single-use.” In most hospitals, medical tools are used once and then thrown away. For something like a cheap plastic syringe, that makes sense. But with a €600 stapler or a €1,300 catheter, the practice becomes both unsustainable and financially wasteful.  That’s where hybrid-use comes in. Instead of discarding the entire device, hospitals can reuse the critical components while protecting them with inexpensive, disposable covers that maintain sterility. The result: less waste, lower cost, and a smarter path to sustainability. In this episode, Dr. Boese joins Lucas to explore what’s driving hospitals toward single-use, how adopting hybrid-use could cut waste from high-value medical devices by up to 75%, and how the next generation of medtech professionals can balance patient safety, performance, and environmental impact. Connect with Axel: LinkedIn: linkedin.com/in/axel-boese-a7b43a188?originalSubdomain=de Axel’s company, MEDICS GmbH: https://medics-md.de/ Connect with us: If you’re a medtech company struggling to make your devices more sustainable, let’s talk: https://lucaspianegonda.clickfunnels.com/optin1756907952105 🎧 Subscribe to the Gradical Podcast for insights on MedTech sustainability, materials, and innovation: 🟣Apple Podcasts: https://podcasts.apple.com/us/podcast/gradical-podcast-the-podcast-about-plastics-in/id1773569554  🟢Spotify:  https://open.spotify.com/show/4vNQ6rPE2CQUGgQtEY3sYq 📺Watch these episodes on YouTube: https://www.youtube.com/@GradicalGmbH 🌍 Learn more about Gradical: https://gradical.ch/ 📩 Work with Lucas and the team: [email protected] Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Arne Jaksch is an expert in toxicology and managing director of his own company Jaksch Life Science Consulting. He supports medical technology, pharmaceutical and chemical companies in the biological and toxicological evaluation of their products. In our discussion we dive deep on how a toxicological risk assessment is performed and what difficulties companies usually face when doing these. This episode was sponsored by Jaksch LifeScience Consulting GmbH - JAKSCH LIFESCIENCE CONSULTING. Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Maximilian Hofmann is Sustainability Manager at Raumedic a leading component supplier, CDMO and medical device manufacturer for some of its products. In the 4 years at Raumedic he established sustainability management systems, ISCC-PLUS certifications for two sites and introduced eco-design into Raumedics development process. Despite all the efforts sustainable products are struggling to take off, in this podcast we want to explore the current challenges of sustainable product development in medtech. Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.

Isobel Filipova is an expert in sustainable design in medical technology and the founder of her own consultancy, where she helps medtech companies redesign medical device for sustainability. With a background in industrial design and medical devices, she has developed a unique approach that balances usability, compliance, and environmental impact. Her work focuses on transforming single-use medical devices into more sustainable multi-use solutions. In our discussion we talk about the holistic understanding of sustainability and the involvement of all stakeholders interests at early stages. Do you enjoy this podcast? Then subscribe, rate it on your platform, and join the discussion on LinkedIn! Your feedback and comments help us improve the podcast and bring you relevant topics. Let’s form a better world with plastics! If you are a Medtech company struggling to make your devices more sustainable, let’s talk—BOOK A CALL HERE.