RQM+
Making MedTech Happen with RQM+
RQM+ is The MedTech CRO – a full-service partner supporting everything from groundbreaking innovation to well-established technologies. Our coordinated and comprehensive solutions are customized to each client’s product and life cycle stage. By aligning strategy and execution in one partner, we help reduce cost, accelerate timelines, and drive more successful outcomes. Visit RQMplus.com to see how we help MedTech companies of all sizes, spanning all device types and therapeutic areas. This podcast provides audio/video we also share on our website and LinkedIn page. Thank you for listening!
Where to listen?
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Episodes
Live! #90 – PMCF Surveys That Survive Scrutiny 03.11.2025 1:11:42
This panel was recorded October 2, 2025. We hope you'll join us live in the future to ask your own questions and participate in the attendee chat! See similar events on demand and read other free MedTech resources at RQMplus.com . PMCF surveys can strengthen your CER and PSUR or create rework. In this 60-minute panel with live audience Q&A, RQM+ leaders from regulatory, clinical,...
Live! #89 – Compliance for EU Market Access with BSI, Brabners, and RQM+ 03.11.2025 1:02:17
This panel was recorded September 18, 2025. We hope you'll join us live in the future to ask your own questions and participate in the attendee chat! See similar events on demand and read other free MedTech resources at RQMplus.com . Manufacturers often focus on MDR or IVDR and miss cross-cutting EU laws that impact CE marking, technical documentation, quality systems, and reporting. A...
Live! #88 – Electric Brains & Regulatory Pains: Accelerate Neurology Innovation, Slash Risk, & Win Approval 17.07.2025 1:09:45
This panel was recorded June 26, 2025. We hope you'll join us live in the future to ask your own questions and participate in the attendee chat! See similar events on demand and read other free MedTech resources at RQMplus.com . Summary Hear leading neurology innovators discuss how to navigate complex regulatory pathways, accelerate approvals, and reduce risk in bringing groundbreaking neu...
Live! #87 – Built for Her: Funding, fixing, and fueling the next era of MedTech 08.04.2025 1:01:09
This panel was recorded 20 March 2025. Please join us live in the future and have your own questions answered! You can sign up for these events and see other resources in the Knowledge Center at RQMplus.com. Women’s health is finally getting the attention it deserves, yet progress is still slowed by gaps in clinical trial diversity, complex regulatory pathways, and funding challenges. In t...
Breast Cancer Panel, Part 3: MedTech Innovations 07.04.2025 26:58
In the final episode of our Breast Cancer Panel, discover how groundbreaking medical technologies and innovative advancements are transforming breast cancer care. Hear firsthand from employees who share their experiences, hopes, and how MedTech is shaping the future of breast cancer treatment and patient outcomes. -- 📲 Follow RQM+ on LinkedIn. 📩...
Breast Cancer Panel, Part 2: Treatment and Advocacy 05.04.2025 33:10
Join us for part two as our courageous panelists discuss their experiences with breast cancer treatment, the importance of self-advocacy, and their involvement in supporting the breast cancer community. This episode highlights practical insights and the incredible strength found through advocacy. -- 📲 Follow RQM+ on LinkedIn. 📩 Subscribe to t...
Breast Cancer Panel, Part 1: Diagnosis and Personal Journeys 04.04.2025 18:57
In this powerful first part of a three-part series, RQM+ employees bravely share their personal journeys from the moment of diagnosis through the emotional and physical challenges they faced. Their stories offer inspiration, resilience, and valuable insights into the realities of breast cancer diagnosis. -- 📲 Follow RQM+ on LinkedIn. 📩 Subscribe...
Weekly Watch #51 (AI-Generated, Subscribe On LinkedIn) 02.04.2025 22:32
This is an experiment and AI-generated audio version of edition #51 of our weekly LinkedIn newsletter, the RQM+ Weekly Watch . This summary is automatically generated and should not be considered a direct statement from RQM+. While we strive for accuracy, please know this summary may contain errors. It's also only a brief snapshot of the material from this week's LinkedIn newsletter...
Weekly Watch #48 (AI-Generated, Subscribe On LinkedIn) 11.03.2025 29:43
This is an experiment and AI-generated audio version of edition #48 of our weekly LinkedIn newsletter, the RQM+ Weekly Watch . This summary is automatically generated and should not be considered a direct statement from RQM+. While we strive for accuracy, please know this summary may contain errors. It's also only a brief snapshot of the material from this week's LinkedIn newsletter,...
Celebrating the Women Who Inspire Us 💜 10.03.2025 13:13
In celebration of International Women's Day , we asked our team to talk about the most influential women in their lives. Their stories had us tearing up, tbh. 🥺 RQM+ applauds ALL women who overcome challenges and inspire others every day. Happy International Women's Day. 💜 Special thanks to our remarkable storytellers: Lisa Sampson Melissa Orenstein Aditi Patel, MS RA LaTya Lindsay Saman...
Weekly Watch #47 (AI-Generated, Subscribe On LinkedIn) 06.03.2025 17:11
This is an experiment and AI-generated audio version of edition #47 of our weekly LinkedIn newsletter, the RQM+ Weekly Watch . This summary is automatically generated and should not be considered a direct statement from RQM+. While we strive for accuracy, please know this summary may contain errors. It's also only a brief snapshot of the material from this week's LinkedIn newsletter, whi...
Live! #86 – PART 2: Medical Device Cybersecurity: Proven Strategies for Connected Devices and SaMD 12.02.2025 1:13:28
This panel was recorded 30 January 2025. Please join us live in the future and have your own questions answered! You can sign up for these events and see other resources in the Knowledge Center at RQMplus.com. As software and connectivity reshape MedTech, implementing effective cybersecurity measures has become business-critical. Join part two of our expert panel for a practical, strategic di...
Live! #85 – Medical Device Cybersecurity: Proven Strategies for Connected Devices and SaMD 19.12.2024 1:03:14
This panel was recorded 12 December 2024. Please join us live in the future and have your own questions answered! You can sign up for these events and see other resources in the Knowledge Center at RQMplus.com. Thank you for tuning in. 🙏 As software and connectivity reshape MedTech, implementing effective cybersecurity measures has become business-critical. Jo...
Live! #84 – Critical Shifts in Biological Evaluation: Inside the New ISO 10993-1 Risk Management Framework 05.12.2024 57:42
This panel was recorded 21 November 2024. Please join us live for future shows for the chance to participate in the chat and ask your own questions! You can sign up for these events and see more free thought leadership content in the Knowledge Center at RQMplus.com. Thank you for tuning in. 🙏 As significant changes to ISO 10993-1 loom on the horizon, manufacturers acr...
Chris Parr, Principal Consultant | Excellence Spotlight 14.11.2024 13:23
Our Excellence Spotlight series celebrates and showcases the remarkable journeys and achievements of RQM+ employees; the same employees who are committed to technical excellence and make a significant impact on our clients. 🌟 𝗘𝘅𝗰𝗲𝗹𝗹𝗲𝗻𝗰𝗲 𝗦𝗽𝗼𝘁𝗹𝗶𝗴𝗵𝘁 interview: Chris A. Parr, PMP With over 20 years in regulatory and quality compliance, Chris exemplifies RQM+'s deep expertise and commitment to our cli...
Carrie Schneider, Principal Consultant | Excellence Spotlight 07.11.2024 14:35
Our Excellence Spotlight series celebrates and showcases the remarkable journeys and achievements of RQM+ employees; the same employees who are committed to technical excellence and make a significant impact on our clients. An 18-yr old McDonald's manager at Purdue University's campus restaurant just so happened to find her 𝗾𝘂𝗮𝗹𝗶𝘁𝘆 𝗺𝗶𝗻𝗱𝘀𝗲𝘁 📋✓ making consistently perfect burgers. Today, Carrie (Ha...
What makes a successful regulatory submission from a clinical trial perspective for IVDs? – MedTech CRO: Regulatory Expertise Series 04.11.2024 9:58
*This video is part of our educational video series on clinical trials. Clips will cover three key areas: clinical trial strategy, clinical trial execution, and regulatory expertise in clinical trials. Please reach out to RQM+ if you need support with clinical trials.* 🎯 𝗪𝗵𝗮𝘁 𝗺𝗮𝗸𝗲𝘀 𝗮 𝘀𝘂𝗰𝗰𝗲𝘀𝘀𝗳𝘂𝗹 𝗿𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝘀𝘂𝗯𝗺𝗶𝘀𝘀𝗶𝗼𝗻 𝗳𝗿𝗼𝗺 𝗮 𝗰𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝘁𝗿𝗶𝗮𝗹 𝗽𝗲𝗿𝘀𝗽𝗲𝗰𝘁𝗶𝘃𝗲 𝗳...
Holly Cotter, Senior Consultant | Excellence Spotlight 28.10.2024 14:53
Our Excellence Spotlight series celebrates and showcases the remarkable journeys and achievements of RQM+ employees; the same employees who are committed to technical excellence and make a significant impact on our clients. 🧗♀️ Our newest 𝗘𝘅𝗰𝗲𝗹𝗹𝗲𝗻𝗰𝗲 𝗦𝗽𝗼𝘁𝗹𝗶𝗴𝗵𝘁 interview is an especially fun one! From National Geographic subscriptions to successfully navigating FDA submissions, meet Senior Consult...
What makes a successful regulatory submission from a clinical trial perspective? (Part 3/3) – MedTech CRO: Regulatory Expertise Series 22.10.2024 9:57
*This video is part of our educational video series on clinical trials. Clips will cover three key areas: clinical trial strategy, clinical trial execution, and regulatory expertise in clinical trials. Please reach out to RQM+ if you need support with clinical trials.* In the final installment of this three-part series, Jaishankar Kutty, Ph. D. concludes...
Live! #83 – Structured Dialogue: How to Engage with Notified Bodies 17.10.2024 1:01:54
This presentation and panel was recorded 4 October 2024. We encourage you to download the slides presented during this session by completing the form on this page . Please join us live for future shows for the chance to participate in the chat and ask your own questions! We generally hold one RQM+ Live! panel discussion per month (in addition to occasional traditional webinars) and...
What makes a successful regulatory submission from a clinical trial perspective? (Part 2/3) – MedTech CRO: Regulatory Expertise Series 15.10.2024 8:35
*This video is part of our educational video series on clinical trials. Clips will cover three key areas: clinical trial strategy, clinical trial execution, and regulatory expertise in clinical trials. Please reach out to RQM+ if you need support with clinical trials.* In part two of a three-part series, Jaishankar Kutty, Ph. D. continues the discussion wi...
Christine Anderson, Principal Consultant | Excellence Spotlight 14.10.2024 11:20
Our Excellence Spotlight series celebrates and showcases the remarkable journeys and achievements of RQM+ employees; the same employees who are committed to technical excellence and make a significant impact on our clients. ⭐ After highlighting many members of our Jordi Labs, an RQM+ Company team in the past two months, we're returning to RA/QA this week. Today we're delighted to share Jaishankar...
What makes a successful regulatory submission from a clinical trial perspective? (Part 1/3) – MedTech CRO: Regulatory Expertise Series 10.10.2024 21:41
*This video is part of our educational video series on clinical trials. Clips will cover three key areas: clinical trial strategy, clinical trial execution, and regulatory expertise in clinical trials. Please reach out to RQM+ if you need support with clinical trials.* In part one of a three part series, Jaishankar Kutty, Ph. D. hosts former FDA lead reviewe...
Michael Louis, Chemist II (Jordi Labs) | Excellence Spotlight 08.10.2024 5:55
Our Excellence Spotlight series celebrates and showcases the remarkable journeys and achievements of RQM+ employees; the same employees who are committed to technical excellence and make a significant impact on our clients. 🧪 Our run of 𝗘𝘅𝗰𝗲𝗹𝗹𝗲𝗻𝗰𝗲 𝗦𝗽𝗼𝘁𝗹𝗶𝗴𝗵𝘁 interviews with our Jordi Labs, an RQM+ Company team members continues with Christine Santagate, RAC chatting with Senior Chemist II and supe...
Best Practices In AE Reporting In Clinical Trials – MedTech CRO: Clinical Trial Execution Series 02.10.2024 13:28
*This video is part of our educational video series on clinical trials. Clips will cover three key areas: clinical trial strategy, clinical trial execution, and regulatory expertise in clinical trials. Please reach out to RQM+ if you need support with clinical trials.* 🚨 Watch our newest video to learn best practices for 𝗮𝗱𝘃𝗲𝗿𝘀𝗲 𝗲𝘃𝗲𝗻𝘁 𝗿𝗲𝗽𝗼𝗿𝘁𝗶𝗻𝗴 𝗶𝗻 𝗰𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝘁𝗿...
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