Do you know the percentage of 510(k)s that are rejected by the FDA the first time? Shockingly, it’s 75%. The vast majority are rejected for poor substantial equivalence, which, as you know, defeats the purpose of the submission in the first place. Today we’re going to talk to Mike Drues, president of Vascular Sciences and regulatory guru, about some common mistakes that can sink your 510(k) submission. Some of the highlights of the show include: ● Jon’s motivation for writing an article about co...
Nov 07, 2019•37 min•Season 1Ep. 53
The topic of Real-World Evidence is generating a lot of discussion lately, especially after the draft guidance was issued last summer and the final guidance was issued in August. So what does Real-world Evidence mean for you and from a regulatory perspective? Today we speak with Mike Drues, President of Vascular Sciences, about how real-world evidence can help you develop products that will improve and save lives. Some of the highlights of the show include: ● Why medical device companies should ...
Nov 07, 2019•36 min•Season 1Ep. 52
Today we’re going to be taking the topic of risk management to the next level. We are talking to Jim Gianoutsos with Regality Consulting. We are going to explore some of the challenges with a company’s approach to manufacturing processes as they apply to risk management. Some of the highlights of the show include: ● Information about Jim’s background and about Regality Consulting. ● Thoughts on how risk is sometimes a box to check rather than an integral part of every discussion and every decisi...
Nov 07, 2019•21 min•Season 1Ep. 54
The topic of human factors can be confusing: How does it relate to design factors and risk? Why is it included in the regulations and how can this factor be handled? On today’s episode, we have Bryant Foster, the Vice President of Research & Design at Research Collective. Bryant applies the principles of cognitive psychology to the design of new technologies and is a great resource on the topic. Some of the highlights of the show include: ● What Bryant does as the VP of Research & Design at Rese...
Nov 07, 2019•36 min•Season 1Ep. 55
This past month, the FDA drafted a guidance on a quick path to approval as an alternative to the 510(k). The question is, is this really anything new? Today, we’ll be talking to Mike Drues, president of Vascular Sciences, and he’s going to help us all understand what’s different about this fast track and how it might benefit you. Some of the highlights of the show include: ● What the new draft is about and how long this fast track has really been around. ● Some thoughts on the ramifications for ...
Nov 07, 2019•29 min•Season 1Ep. 56
Do you have a firm grasp and understanding of what substantial equivalence means in regards to the 510(k)? Many don’t understand it; the evidence is the large percentage of submissions that are rejected due to a lack of demonstrating substantial equivalence. Today we’re talking with Mike Drues, President of Vascular Sciences about demonstrating substantial equivalence, so if you’re not rock-solid on the concept, you won’t want to miss this episode. Some of the highlights of the show include: ● E...
Nov 07, 2019•34 min•Season 1Ep. 57
What are the most common problems with the CAPA process? Today, frequent guest Mike Drues, president of Vascular Sciences and Jon are going to dive into that question and get you the answers you need and want. SOME OF THE HIGHLIGHTS OF THE SHOW INCLUDE: ● Why the CAPA process is such a big issue within the industry and why Jon wrote a column on it. ● What businesses are doing instead of focusing on CAPA and why this is one of the major problems with the process, as well as why a cross-functional...
Nov 07, 2019•40 min•Season 1Ep. 59
Are you ready for audits? ISO? FDA? Is your quality management system working the way you want it to? Is it still just a checkbox activity? Or, are you ready to elevate yourself to be a true quality professional? A quality management system should help us run our business better and produce safer medical devices. It should be built well and run well - effective and efficient. On today’s episode, we have Larry Mager, a senior advisor for UL EHS Sustainability. He shares a tool he developed called...
Nov 07, 2019•25 min•Season 1Ep. 58
When it comes to quality management compliance, would you consider yourself a box checker or a true quality professional? On today’s episode, we talk with Mike Drues, president of Vascular Sciences, about what it means to be a true quality professional and how to ensure your quality management system is effective and benefits patients. Do you want to offer medical devices that improve your patients’ quality of life? Don’t wait until an FDA audit to make changes or try and fix problems. Some of t...
Nov 07, 2019•35 min•Season 1Ep. 60
When it comes to 13485:2016, are you scrambling to meet requirements? Are you trying to figure out the how, what, or when regarding its timeline? Or, maybe you just don’t know what you need to do. You are not alone because a lot of companies are behind. Don’t wait until it is too late. Now is the time to take action. Today’s guest is Kyle Rose, president of Rook Quality Systems, which helps companies achieve 13485 certification by using the Greenlight Guru’s Quality Management Software platform....
Nov 07, 2019•28 min•Season 1Ep. 62
When developing a new medical device, do you try to figure out the fastest and simplest way to get your product to market? As a product developer, do you explore a regulatory path? Or, are you afraid that may kill your idea? Mike Drues, president of Vascular Sciences, is with us today to do some premarket approval (PMA) myth busting and describes why a PMA path may not be as scary as you think. Some of the highlights of the show include: ● PMAs are reserved for the highest risk devices (Class II...
Nov 07, 2019•40 min•Season 1Ep. 63
Students offer hope for our future. They will be developing products that can save our lives, or at least improve our quality of life. We need to give them as much guidance and advice as possible. On today’s episode, we have Associate Professor Andrew DiMeo, who shares his mission and what he is trying to do with the biomedical program at the University of North Carolina and North Carolina State University. Some of the highlights of the show include: ● Andrew’s biomedical product development cou...
Nov 07, 2019•33 min•Season 1Ep. 61
The FDA announced a new proposal regarding the bundling of device malfunctions when Medical Device Reporting (MDR). On today’s episode, we have Mike Drues, president of Vascular Sciences, to help us dive into the impact of this proposal and the safety of medical devices. The FDA proposal’s benefits probably outweigh the risks and should be implemented on a small scale. Some highlights of the show include ●Depending on the severity of the malfunction, you are given a specified amount of time to r...
Nov 07, 2019•31 min•Season 1Ep. 65
Do you know how to use the FDA’s abbreviated 510(k)? Since only 2 percent of 510(k)s have gone the abbreviated path, it’s likely an accurate assumption that many don’t know how to use it. Today, Mike Drues, the president of Vascular Sciences, and Jon Speer are going to delve into the abbreviated 510(k) path and how it can benefit you. Some of the highlights of the show include: ● The three principal types of 510(k)s and how they differ from one another. ● The crux of the abbreviated 510(k) and h...
Nov 07, 2019•43 min•Season 1Ep. 64
As companies transition from being a start-up or small company to a more established business and bring new medical devices to market, they tend to not put a lot of thought into their processes, systems, and approaches for regulatory strategies and quality systems. Regardless of the shape and size of your company, these factors are foundational to the growth and success of your business. Host Jon Speer and Mike Drues of Vascular Sciences discuss key tips on what to think about regarding regulato...
Nov 07, 2019•38 min•Season 1Ep. 67
Have you ever designed a medical device that has electrical components? Was it frustrating to go through the electrical safety testing - the IEC 60601 standards? Claus Roemer Andersen, a compliance expert from Roemer Consulting, shares his experiences and advises us on how to design for compliance with IEC 60601. After all, a lack of electrical compatibility can be detrimental to medical devices and the patients who use them. IEC 60601 documentation is a lot to digest, which is a major challenge...
Nov 07, 2019•34 min•Season 1Ep. 66
