DCN Dx Expert Insights is a podcast for teams developing and commercializing in vitro diagnostics. Each episode brings together scientists, clinical researchers, regulatory specialists, manufacturing experts, and industry leaders to examine the decisions that determine whether an IVD program reaches the market.
Topics include assay development, clinical evidence, regulatory strategy, biospecimens, manufacturing, scale-up, product development, and commercialization.
Subscribe to Expert Insights on Spotify, Apple Podcasts, or your preferred platform, and visit dcndx.com for additional tools and resources.
LISTEN AND FOLLOW
Spotify: https://open.spotify.com/show/16GcmTI4U7dhzKSQe0mUhO
Apple Podcasts: https://podcasts.apple.com/us/podcast/dcn-dx-expert-insights/id1793226272
Subscribe on YouTube: https://www.youtube.com/channel/UCgMr7XR64b1Q1_0nG-X8b1Q?sub_confirmation=1
MORE FROM DCN DX
Explore IVD articles, podcast transcripts, and technical resources: https://dcndx.com/insights/
Learn more about DCN Dx: https://dcndx.com/
Discuss your IVD program with our team: https://dcndx.com/contact/
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Wellness or Medical Device? FDA's 2026 Wellness Guidance and the WHOOP Warning Letter
Season 3 · Episode 11
Friday, September 4, 2026 • Duration 43:47
In July 2025, FDA told WHOOP that its Blood Pressure Insights feature was an unauthorized medical device. WHOOP disputed FDA’s position and kept selling it. In January 2026, while the dispute was still open, FDA reissued its general wellness guidance. FDA closed the warning letter in June after WHOOP modified the feature and its labeling.
Working through this question for your own product? Request a call with DCN Dx:
https://dcndx.com/wellness
In this episode of Expert Insights, Emily Friedland talks with Blythe Karow, Founder and CEO of The Karow Advisory Group, and Dan Simpson, RAC, Director of Regulatory Affairs at DCN Dx, about where a product intended for wellness becomes a regulated medical device and why the same line-drawing questions apply to at-home diagnostics. They discuss how risk, intended use, claims, form factor, and presentation can shape FDA’s view of a product.
DCN Dx offers a fixed-fee Wellness Regulatory Assessment. In two to four weeks, you receive a written assessment of how FDA’s current general wellness policy may apply, the likely regulatory path, and whether FDA contact is warranted.
WHAT YOU’LL HEAR IN THIS EPISODE
- What FDA’s January 2026 guidance clarified for noninvasive sensing functions such as blood pressure, and Blythe’s view of its effect on the modified WHOOP feature
- Why a patch that uses a subcutaneous needle falls outside FDA’s low-risk general wellness policy, whatever the marketing language
- Dan’s experience with FDA 513(g) responses for at-home lateral flow assays proposed for wellness uses
- How a claims matrix, a tiered review process, and rules for influencer content can keep marketing language from crossing into medical-device claims
- Blythe’s read on the WHOOP warning letter, the stoplight-color dispute, and the risks of bundling a wellness feature with two cleared medical-device features
Full transcript and show notes:
https://dcndx.com/insights/technically-wellness-gray-zone-between-consumer-health-regulated-diagnostics/
GUESTS
Blythe Karow | Founder and CEO, The Karow Advisory Group
Blythe is a MedTech strategist with twenty-five years across medical devices, wearables, and regulated health technology. She founded The Karow Advisory Group, where she advises CEOs, investors, and executive teams on product strategy, commercialization, and U.S. market entry, from early-stage startups to Fortune 50 companies. She was previously Co-founder and CEO of Evren Technologies, where she led the Phoenix transcutaneous vagus nerve stimulation device to FDA Breakthrough Device Designation in 2021, and Head of Digital Health Strategy for spinal cord stimulation at Boston Scientific. She writes The Device Files, a widely read Substack on MedTech strategy and the regulation of wearables and consumer health, whose readership grew sharply through her coverage of the WHOOP case. She is an Entrepreneur in Residence at Yale and holds a biomedical engineering degree from Johns Hopkins and an MBA from the University of Virginia’s Darden School.
Dan Simpson, RAC | Director of Regulatory Affairs, DCN Dx
Dan is Director of Regulatory Affairs at DCN Dx and a RAC-credentialed, ASQ-certified medical device auditor with more than 15 years in IVD and medical device regulatory and quality roles. Before DCN Dx he led regulatory affairs at ERI Group and spent 14 years running quality and regulatory affairs at Corgenix Medical Corporation. He works with IVD manufacturers on FDA 510(k), De Novo, and PMA submissions as well as IVDR conformity assessment, across point-of-care, OTC, companion diagnostics, and high-complexity assays.
HOST
Emily Friedland | VP of Clinical Research, DCN Dx
ABOUT DCN DX EXPERT INSIGHTS
DCN Dx Expert Insights examines the technical, regulatory, clinical, and manufacturing decisions that shape the development and commercialization of in vitro diagnostics.
Before the Protocol: What Sponsors Miss About Sites and Human Factors
Season 3 · Episode 10
Wednesday, August 5, 2026 • Duration 56:40
A site management CEO and a human factors specialist on what sponsors miss before a diagnostic study ever starts.
Most conversations about IVD clinical research happen from the sponsor’s side of the table. This episode flips that. Emily Friedland, VP of Clinical Research at DCN Dx, sits down with Missy Farrell, founder and CEO of , and Karen Seidler, Ph.D, CEO and Principal at , to talk about the two stages that happen before a protocol is finalized: the human factors work that determines whether real users can operate a device safely, and the site feasibility work that determines whether a clinic can deliver the study a sponsor designed on paper.
For sponsors and CROs, the payoff is practical. Missy explains why prevalence numbers on a feasibility questionnaire routinely mislead sponsors about who a site can enroll, and Karen walks through why combining a human factors validation study with a clinical study creates logistical problems that are hard to see coming. Together they make the case for treating these two disciplines as sequential, not overlapping, and for asking sites and device teams sharper questions much earlier in development.
ABOUT DCN DX EXPERT INSIGHTS
DCN Dx Expert Insights examines the technical, regulatory, clinical, and manufacturing decisions that shape the development and commercialization of in vitro diagnostics.
LISTEN AND FOLLOW
Spotify: https://open.spotify.com/show/16GcmTI4U7dhzKSQe0mUhO
Apple Podcasts: https://podcasts.apple.com/us/podcast/dcn-dx-expert-insights/id1793226272
Subscribe on YouTube: https://www.youtube.com/channel/UCgMr7XR64b1Q1_0nG-X8b1Q?sub_confirmation=1
MORE FROM DCN DX
Explore IVD articles, podcast transcripts, and technical resources: https://dcndx.com/insights/
Learn more about DCN Dx: https://dcndx.com/
Discuss your IVD program with our team: https://dcndx.com/contact/
Where Programs Fail: Bridging Assay Development and Manufacturing for Lateral Flow
Season 3 · Episode 9
Thursday, July 23, 2026 • Duration 41:37
Your lateral flow assay performs at the bench. Will that performance hold on the manufacturing line?
Manufacturing introduces conditions the assay may not have faced at the bench. Reagent delivery must remain consistent throughout longer runs, while materials move under tension on production equipment. Changes in dispensing and drying can expose signal variation, nonspecific binding, material failures, or yield loss.
For immunoassay developers, finding those problems after the assay design is locked can send the program back into development. The better time to address them is during development, while the chemistry, materials, and process can still be evaluated together.
In this episode of Expert Insights, DCN Dx Chief Operating Officer Pat Vaughan, Ph.D., who leads assay development, engineering, and manufacturing operations, joins host Trevor Brown, M.Sc., Chief Revenue Officer, to explain what changes between the bench and the manufacturing line. They discuss what immunoassay developers should evaluate before the design is locked and how assay scientists and manufacturing engineers can work together from the start.
ABOUT DCN DX EXPERT INSIGHTS
DCN Dx Expert Insights examines the technical, regulatory, clinical, and manufacturing decisions that shape the development and commercialization of in vitro diagnostics.
LISTEN AND FOLLOW
Spotify: https://open.spotify.com/show/16GcmTI4U7dhzKSQe0mUhO
Apple Podcasts: https://podcasts.apple.com/us/podcast/dcn-dx-expert-insights/id1793226272
Subscribe on YouTube: https://www.youtube.com/channel/UCgMr7XR64b1Q1_0nG-X8b1Q?sub_confirmation=1
MORE FROM DCN DX
Explore IVD articles, podcast transcripts, and technical resources: https://dcndx.com/insights/
Learn more about DCN Dx: https://dcndx.com/
Discuss your IVD program with our team: https://dcndx.com/contact/
Off the Patchwork: What a Connected Platform Lets a CRO Do for Sponsors
Season 3 · Episode 8
Wednesday, July 1, 2026 • Duration 44:07
Many IVD clinical studies still run on a patchwork of disconnected tools: a file share here, a spreadsheet there, a separate system for clinical operations and another for the data. The handoffs between them put time, money, and clean data at risk. Since 2021, DCN Dx has been developing something different: one connected platform on Veeva, with the electronic trial master file, EDC, and CTMS all talking to each other.
In this candid discussion, host Emily Friedland (VP of Clinical Research, DCN Dx) sits down with two of the people who built and run it, Thomas Martinache (Associate Director, Data Management, DCN Dx) and Jill Hutton-Pugh (Clinical Trial Manager, DCN Dx), along with John Acampado (Senior Director of Clinical Strategy, Veeva). They get into what the old patchwork model cost, how DCN put the connected platform together piece by piece, and, most of all, what it changes for the sponsors who hire them: faster study startup, real-time visibility into enrollment and milestones, cleaner data with fewer manual handoffs, and a compliant foundation that an emerging IVD or MedTech company can grow on.
The conversation leads into the team’s Veeva webinar on July 15, Platform Over Patchwork: How Consolidation Drives CRO Efficiency, where DCN Dx will share its journey of moving onto a single platform to drive operational efficiency in high-intensity trials, including 60% improvement in IMV preparation, 45% reduction in build time, and 30% faster study closeout. Register for that webinar here: https://veeva.zoom.us/webinar/register/WN_m8krwBa4RLCnK17MpVZVCw#/registration
Emily Friedland | VP of Clinical Research, DCN Dx
Emily Friedland is Vice President of Clinical Research at DCN Dx, where she leads the company's clinical operations across IVD and medical device studies. She has more than two decades in clinical research, including a turn as Global Director of Clinical Operations at Teleflex and earlier roles at Singulex, Grifols, Celera, and Roche, spanning infectious disease, genetic testing, and women's health. She holds a B.S. from Virginia Tech and is based at DCN Dx's headquarters in Carlsbad, California.
John Acampado | Sr. Director, Clinical Strategy, Veeva MedTech
John leads strategy at Veeva MedTech, focused on helping CROs and sponsors build connected, scalable clinical solutions across device and diagnostics. He came to Veeva from the sponsor side, including time at Becton Dickinson, and brings that experience to Veeva’s MedTech product direction and to his work on the MDIC IVD standards working group.
Jill Hutton-Pugh | Clinical Trial Manager, Clinical Operations, DCN Dx
Jill Hutton-Pugh is a Clinical Trial Manager in Clinical Operations at DCN Dx and the clinical team's lead on its connected Veeva platform. She has two spent decades in clinical research spanning IVD, clinical safety, and pharmaceutical strategy, with study experience across infectious disease, HIV, interventional cardiology, and hypertension. Known for getting multidisciplinary teams aligned and projects finished on time, she has held clinical operations and monitoring roles at Teleflex, Conformal Medical, and Essential Medical, with earlier years at Merck in hospital sales and pricing. She holds a B.S. in microbiology from Ohio State University and pursued graduate business studies at both Ohio State and Temple.
Thomas Martinache | Associate Director of Data Management, DCN Dx
Thomas Martinache is Associate Director of Data Management at DCN Dx, with 15 years in clinical data management. He spent much of his career supporting CROs and sponsors in cardiology and oncology, in roles at Teleflex, HeartFlow, and BioClinica, before turning his focus to IVD. At DCN Dx he leads the data management team and the connected Veeva platform that runs across the firm's studies, supporting sponsors from protocol design and site selection through final statistical reporting and regulatory submissions.
Stuck in a Holding Pattern: The IVDR Revision and Planning for Two Markets at Once
Season 3 · Episode 7
Wednesday, June 10, 2026 • Duration 35:59
The 2026 IVDR transition deadlines are here, and a lot of IVD companies are sitting still. After the European Commission proposed a revision to the regulation in December 2025, many manufacturers are waiting to see what survives before they file. By late May, notified bodies reported that submissions had slowed so much that some have cut staff and a few may close. The old IVDD deadlines keep running out, the dates for higher-risk classes have already passed, and the Commission's message has been consistent: no more extensions.
Dan Simpson, Director of Regulatory Affairs at DCN Dx, and Sarah Barchard, Senior Clinical Trials Manager at DCN Dx, talk through what the waiting costs a company that has to sell in both the EU and the US, and why it pays to plan for both markets at the same time instead of one after the other.
Dan takes the regulatory side: where the two systems differ, and how those differences shape design and development long before anyone files. Sarah takes the clinical side: where EU and US requirements pull in different directions during analytical and clinical work, and what it takes to run studies that hold up in both places.
This conversation leads into their RAPS sponsored webcast, The IVDR Transition in 2026: Parallel Regulatory Planning for EU and US Market Entry, on June 17 at 12pm ET. It's free, and you can register through RAPS. Dan and Sarah will walk through the case studies behind what they discuss here.
Register: https://www.raps.org/learn-develop/events/sponsored-webcast-the-ivdr-transition-in-2026-parallel-regulatory-planning-for-eu-and-us-market-entry.html
Talk through your own program: dcndx.com/contact
ABOUT DCN DX EXPERT INSIGHTS
DCN Dx Expert Insights examines the technical, regulatory, clinical, and manufacturing decisions that shape the development and commercialization of in vitro diagnostics.
LISTEN AND FOLLOW
Spotify: https://open.spotify.com/show/16GcmTI4U7dhzKSQe0mUhO
Apple Podcasts: https://podcasts.apple.com/us/podcast/dcn-dx-expert-insights/id1793226272
Subscribe on YouTube: https://www.youtube.com/channel/UCgMr7XR64b1Q1_0nG-X8b1Q?sub_confirmation=1
MORE FROM DCN DX
Explore IVD articles, podcast transcripts, and technical resources: https://dcndx.com/insights/
Learn more about DCN Dx: https://dcndx.com/
Discuss your IVD program with our team: https://dcndx.com/contact/
QMSR Is in Effect: What IVD Manufacturers Still Need to Do
Season 3 · Episode 6
Friday, May 8, 2026 • Duration 36:29
In this episode, Emily Friedland, VP of Clinical Research at DCN Dx, talks with two guests who come at QMSR from different directions: the regulatory strategy side and the quality systems implementation side.
Dan Simpson, RAC, Director of Regulatory Affairs at DCN Dx, covers the regulatory framing: what changed with the QMSR transition, how to map an ISO 13485-based QMS against QMSR’s U.S.-specific requirements, and what FDA’s updated inspection approach under CP 7382.850 means for how teams document and maintain QMS records.
Kevin Gunning, Principal Consultant at Gunning Quality Systems LLC, brings the quality systems implementation perspective: what it takes to build and maintain a QMS that holds up under QMSR, how organizations should think about the practical work of a gap assessment and remediation, and what teams with established ISO 13485 systems often overlook when they assume the transition is “mostly handled.” Kevin has spent more than 25 years implementing and managing quality systems at IVD and medical device companies, and has extensive firsthand experience on both sides of FDA and ISO audits and inspections.
Together, Dan and Kevin cover the four gap areas that matter most for IVD manufacturers, what FDA can now request during an inspection that was previously off-limits, and how to scope a proportional remediation effort.
Read the companion article here: https://dcndx.com/insights/qmsr-ivd-manufacturers-gaps-iso-13485/
ABOUT DCN DX EXPERT INSIGHTS
DCN Dx Expert Insights examines the technical, regulatory, clinical, and manufacturing decisions that shape the development and commercialization of in vitro diagnostics.
LISTEN AND FOLLOW
Spotify: https://open.spotify.com/show/16GcmTI4U7dhzKSQe0mUhO
Apple Podcasts: https://podcasts.apple.com/us/podcast/dcn-dx-expert-insights/id1793226272
Subscribe on YouTube: https://www.youtube.com/channel/UCgMr7XR64b1Q1_0nG-X8b1Q?sub_confirmation=1
MORE FROM DCN DX
Explore IVD articles, podcast transcripts, and technical resources: https://dcndx.com/insights/
Learn more about DCN Dx: https://dcndx.com/
Discuss your IVD program with our team: https://dcndx.com/contact/
Specimen Strategy Is Development Strategy (And Why "We'll Source It Later" Fails)
Season 3 · Episode 5
Friday, April 3, 2026 • Duration 36:19
Specimen strategy is one of the most common sources of avoidable delay in IVD development. Teams that defer specimen decisions until after the evidence plan is set tend to discover the mismatch at the worst possible time: during analytical validation, clinical performance work, or submission prep.
In this episode of Expert Insights, Mitzi Rettinger talks with Jim Boushell, Senior Vice President of Biospecimens at DCN Dx, about what experienced teams define early so their specimen sets and data packages hold up under regulatory scrutiny.
Jim has spent decades building biorepositories and supporting diagnostic developers. The conversation covers how to align a specimen plan to an evidence plan from the start, where programs get burned on matrix selection, prevalence, comparator methods, metadata, and pre-analytical handling, and what a high-integrity, audit-ready data package should contain.
Topics in this episode:
-What "specimen strategy" includes and why it is separate from procurement
-Early warning signs that a program is headed for specimen-related delays
-The most common failure modes in specimen planning
-The minimum inputs a developer needs to define before designing a collection
-When banked specimens make sense versus prospective collection
-How DCN Dx runs prospective collections: specimen types, special handling, site operations, and data packages
-What "audit-ready" documentation means for IVD submissions
-Where handoffs fail when collections, assay development, and clinical execution are split across multiple groups
Learn more about DCN Dx's prospective biospecimen collections at dcndx.com/biospecimen-service
ABOUT DCN DX EXPERT INSIGHTS
DCN Dx Expert Insights examines the technical, regulatory, clinical, and manufacturing decisions that shape the development and commercialization of in vitro diagnostics.
LISTEN AND FOLLOW
Spotify: https://open.spotify.com/show/16GcmTI4U7dhzKSQe0mUhO
Apple Podcasts: https://podcasts.apple.com/us/podcast/dcn-dx-expert-insights/id1793226272
Subscribe on YouTube: https://www.youtube.com/channel/UCgMr7XR64b1Q1_0nG-X8b1Q?sub_confirmation=1
MORE FROM DCN DX
Explore IVD articles, podcast transcripts, and technical resources: https://dcndx.com/insights/
Learn more about DCN Dx: https://dcndx.com/
Discuss your IVD program with our team: https://dcndx.com/contact/
Automation Beyond the Strip: Building Repeatable Rapid Test Production with KinBio
Season 3 · Episode 4
Wednesday, March 18, 2026 • Duration 16:07
As rapid diagnostic programs transition from R&D to scaled production, small sources of variation can quickly become major risks. In this episode of Expert Insights, Mitzi Rettinger, Chief Revenue Officer at DCN Dx, sits down with Daniel Levenson, Business Development Manager at KinBio, to discuss what truly changes when you move from manual processes to automated, repeatable manufacturing systems.
The conversation goes beyond dispensing and strip cutting to address the often-overlooked bottlenecks in vial filling, kit assembly, packaging, and sealing. Daniel explains how throughput challenges, moisture control, seal integrity, and alignment issues can affect lot consistency, and why automation must extend across the full production workflow, not just the strip.
They also explore the role of in-line vision systems and defined critical-to-quality attributes (CTQs) in reducing manufacturing risk. As multiplex tests and more complex point-of-care formats become more common, developers must design flexibility, inspection, and traceability into their processes early. The result: fewer surprises, stronger process control, and a clearer path to scalable production.
Guest
Daniel Levenson is Business Development Manager at Shanghai Kinbio Tech Co., Ltd. He brings years of hands-on technical experience in rapid test manufacturing to his work supporting developers scaling into automated production.
ABOUT DCN DX EXPERT INSIGHTS
DCN Dx Expert Insights examines the technical, regulatory, clinical, and manufacturing decisions that shape the development and commercialization of in vitro diagnostics.
LISTEN AND FOLLOW
Spotify: https://open.spotify.com/show/16GcmTI4U7dhzKSQe0mUhO
Apple Podcasts: https://podcasts.apple.com/us/podcast/dcn-dx-expert-insights/id1793226272
Subscribe on YouTube: https://www.youtube.com/channel/UCgMr7XR64b1Q1_0nG-X8b1Q?sub_confirmation=1
MORE FROM DCN DX
Explore IVD articles, podcast transcripts, and technical resources: https://dcndx.com/insights/
Learn more about DCN Dx: https://dcndx.com/
Discuss your IVD program with our team: https://dcndx.com/contact/
Point-of-Care in 2025: Lateral Flow Grew Up. Where Will the Technology Go Next?
Season 3 · Episode 3
Thursday, February 19, 2026 • Duration 42:32
In this episode of Expert Insights, DCN Dx’s Mitzi Rettinger speaks with Dr. Pat Vaughan, DCN Dx’s Chief Operating Officer, about what point-of-care really meant in 2025, how development expectations have shifted, and his predictions for what 2026 will bring.
Drawing from Pat’s recent article and hands-on experience across assay development, engineering, clinical research, and manufacturing, the discussion breaks down how modern lateral flow programs are being designed around readers, software, data pathways, and real-world use.
The episode explores what this shift changes for teams defining new development programs, including how early design inputs affect performance targets, usability, regulatory strategy, and scalability. Pat also compares today’s realities with predictions he made in his 2024 year-in-review, highlighting where the industry moved faster (and slower) than expected.
What you’ll hear in this episode:
-Why lateral flow is now an integrated system, not just a strip with visual interpretation
-How reader-assisted and semi-quantitative performance are shaping new development programs
-Where teams underestimate complexity when moving from prototype to regulated product
-What “born digital” results and AI-enabled interpretation require from a regulatory and operational standpoint
Guest:
Dr. Pat Vaughan is Chief Operating Officer at DCN Dx, where he works across assay development, engineering, clinical research, regulatory strategy, and manufacturing to support point-of-care diagnostic programs from concept through deployment.
ABOUT DCN DX EXPERT INSIGHTS
DCN Dx Expert Insights examines the technical, regulatory, clinical, and manufacturing decisions that shape the development and commercialization of in vitro diagnostics.
LISTEN AND FOLLOW
Spotify: https://open.spotify.com/show/16GcmTI4U7dhzKSQe0mUhO
Apple Podcasts: https://podcasts.apple.com/us/podcast/dcn-dx-expert-insights/id1793226272
Subscribe on YouTube: https://www.youtube.com/channel/UCgMr7XR64b1Q1_0nG-X8b1Q?sub_confirmation=1
MORE FROM DCN DX
Explore IVD articles, podcast transcripts, and technical resources: https://dcndx.com/insights/
Learn more about DCN Dx: https://dcndx.com/
Discuss your IVD program with our team: https://dcndx.com/contact/
The DCN Dx Model: Integration, Scale, and What Comes Next with DCN Dx CEO Charlie Mamrak
Season 3 · Episode 2
Friday, February 6, 2026 • Duration 17:02
A DCN Dx Expert Insights conversation with Charlie Mamrak, CEO at DCN Dx, hosted by Mitzi Rettinger.
Most IVD programs don’t lose months because a single experiment failed. They lose months at the seams: development to clinical, clinical to regulatory, scale-up to routine manufacturing, and specimen strategy to evidence generation.
In this episode, DCN Dx CEO Charlie Mamrak explains the business decisions behind DCN’s integrated services model, why biospecimens became a priority for IVD developers, and how he evaluates what to build, buy, or collaborate on next. This is a strategy conversation, designed for teams who care about execution, risk, and real-world constraints of diagnostics services companies.
What you’ll hear in this episode:
-Why integration is the point: what changes when rapid testing CDMO capabilities and IVD clinical research (CRO) services operate as one platform.
-Why biospecimens: what DCN has heard from customers, what offering prospective biospecimens collections changes for IVD developers, and how it fits the broader integration plan for DCN Dx.
-Workforce development as strategy: why DCN teaches the Basic Lateral Flow Course.
-Build vs. buy vs. collaborate: a CEO framework for deciding when new capabilities reduce friction for customers and align to corporate core values vs. simply expanding the menu of services.
Guest:
Charlie Mamrak is CEO of DCN Dx. He joined DCN Dx in 2020 after leading multiple diagnostics and life science tools companies, including SeraCare Life Sciences.
ABOUT DCN DX EXPERT INSIGHTS
DCN Dx Expert Insights examines the technical, regulatory, clinical, and manufacturing decisions that shape the development and commercialization of in vitro diagnostics.
LISTEN AND FOLLOW
Spotify: https://open.spotify.com/show/16GcmTI4U7dhzKSQe0mUhO
Apple Podcasts: https://podcasts.apple.com/us/podcast/dcn-dx-expert-insights/id1793226272
Subscribe on YouTube: https://www.youtube.com/channel/UCgMr7XR64b1Q1_0nG-X8b1Q?sub_confirmation=1
MORE FROM DCN DX
Explore IVD articles, podcast transcripts, and technical resources: https://dcndx.com/insights/
Learn more about DCN Dx: https://dcndx.com/
Discuss your IVD program with our team: https://dcndx.com/contact/
