Medical devices

Quality, Mac vs. PC, and my eyes

The largest argument in the internet isn't Obama's healthcare plan, whether the Yankees should lose the World Series, or why does gas cost so much. No, it's Mac vs. PC. Across the internet, it's the argument that gobbles up bandwidth in a never-ending discussion. There are several websites that keep tabs on new technology. They are interesting if you want to read about a new mobile phone or a new rice harvesting robot. But whenever they talk about a new product from Apple or something from Microsoft, there's dozens, if not hundreds, of comments about one or the other. Then it gets personal.

I find these discussions amusing, because the arguments on both sides fall a little flat. Now, this website is hosted on Mac servers. And I wrote and designed this website on a Mac with a Mac-only web design program. So, you might think I'm biased, which I am. I'm not going to get into all the arguments between the two devices, but Windows based computers vastly outsell Macs. Most Mac users tend to very loyal to the brand for a number of valid reasons, including ease-of-use and fewer problems. Most PC users tend to look for lower prices without regards to the brand. However, there is a small, but vocal, group of very technical individuals who are loyal to PC's because they are more adept at maximizing the potential of PC's. I'm not convinced of all of their arguments, but they certainly are.
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The value of blood-glucose monitoring

One of the paradigms of managing patients with Type II diabetes includes regular home testing of blood glucose levels using one of the widely available blood glucose monitors. The American Diabetes Association, one of the leading organizations that advocate for and provide information about diabetes, recommends home glucose monitoring for patients who have diabetes and are:

  • taking insulin or diabetes pills
  • on intensive insulin therapy
  • pregnant
  • having a hard time controlling your blood glucose levels
  • having severe low blood glucose levels or ketones from high blood glucose levels
  • having low blood glucose levels without the usual warning signs

These are probably good recommendations, based on good evidence. Controlling blood glucose in those patients with Type 2 diabetes has strong positive benefits for reducing risks of chronic and acute diseases, such as
peripheral artery disease, hypertension, diabetic dyslipidemia, heart attack and stroke.

Recently, a
clinical trial published in the British Medical Journal analyzed the medical usefulness of home blood glucose monitoring in patients with Type II diabetes. The trial was well designed enrolling 184 individuals with recently diagnosed type 2 diabetes mellitus. The patients were randomized into two groups: one that utilized a monitor and one that did not. The patients were observed for one year. Read More...

Increased FDA scrutiny of medical devices

In the early 1990’s, Congress directed the US Food and Drug Administration (FDA) to gather more rigorous evidence before a they give approval to manufacturer to market medical devices that were considered the most risky, a category known as Class III devices. The FDA never implemented the law, and several hundred Class III devices were approved by the FDA based on a less rigorous path using a 510(k), which allows the manufacturer to establish that their products are “substantially equivalent” to products marketed before 1976. Early this year, the Government Accounting Office (GAO) issued a report that stated these conclusions about the process:

FDA has stated that eventually all class III devices will require FDA approval through the PMA process and FDA officials reported that the agency is committed to addressing this issue, but the agency has not specified time frames for doing so. Without FDA action, the remaining preamendment class III device types—including device types that FDA identified in 1994 as presenting an unreasonably high risk to public health—may enter the U.S. market through FDA’s less stringent premarket notification process.


The recommended that the FDA take immediate steps to issue regulations for all of the Class III devices that were allowed to enter the market through the 510(k) process. They directed the FDA to either reclassify each Class III device into either Class I or Class II (based on scientific evidence only) or require that it remain Class III. Those products that remain in Class III will require a new approval through the
Pre-Market Approval (PMA) process, the most stringent for medical devices. Read More...

Point-of-care diagnostics and the flu

I am enamored of the point-of-care (POC) diagnostics market. It is clear that these tests bring benefits to patients, physicians and managed care. Influenza A H1N1 (apparently, the pork industry does is not fond of the swine flu label) may open a huge opportunity for rapid testing for flu.

Quidel Corporation (NASDAQ GS: QDEL) manufactures and markets a rapid (less than 10 minutes from swab to results) diagnostic kit for Influenza A and B (and differentiates between the two). As Quidel states, they are not sure if it detects the swine flu strain. The test should be used for any patients that present with influenza symptoms, because a positive result may rule out other types of infections (and should involve contacting a local health department), although a negative result (if the test does not identify the swine flu type) may not rule out the disease. Read More...

Denialism and pseudoscience

Today, I commented to a blog entry at Beyond the Short Coat, which is one of my daily stops on the medical blogosphere. The author, like a lot of bloggers in the medical arena, has been taking on the world of medical woo, that is, those ideas in medicine that completely lack verifiability and scientific credibility. I have a similar disdain for woo, for essentially the same reasons as the physicians who write in those various blogs. Mostly, they are troubled that patients turn to these useless therapies because they may not be getting adequate medical care, or even that those fake therapies may have terrible consequences for the patient. I take it a step further in that I believe that this woo has a substantial economic consequence with increased costs for patients, providers, and third-party payors. Read More...

Scientific medicine and Big Pharma

I keep reading across the blogosphere that Big Pharma (for the sake of this discussion, defined as all medical products companies, including ones that don’t manufacture or market pharmaceuticals) somehow blocks either positive or negative results to further their profits. The accusations come from a wide variety of sources, some of the more vocal being the anti-science proponents, such as the anti-vaccination movement. Utilizing an ad hominem argument of personalizing the issues and then attacking the motives or character of others, usually those who dispute the claims made by pseudoscience. Read More...

Point-of-care diagnostic–market opportunity

Over the past year, I’ve been observing the growth of a class of medical products called point-of-care diagnostic testing. These tests are easy to use, are accurate, and provide rapid results for the patient and clinician. Some are intended for home use, but the market growth is in the physician office, hospitals (especially the point of entry such as emergency departments), managed care, and other clinical areas. Several companies are in the market, including Quidel, Inverness Medical Innovations, OraSure, and Bayer. The diagnostic tests, manufactured and marketed by these companies (and several others, too numerous to mention), are used mainly for drug abuse screening, cholesterol levels, infectious diseases (including HIV), urine chemistry, blood glucose, hemoglobin A1C, prothrombin time, cancer screening, fecal occult blood, pregnancy, and other areas of clinical diagnostics. The tests can provide results in a manner of minutes, rather than sending the patient to a laboratory to await results hours or days later. Read More...

Strength of the medical products industry

There continues to be quite a bit of anecdotal data that the medical products industry, including medical device, biotechnology, and pharmaceutical sectors of the industry, is healthy and employment is running counter to the recession. I do not have definitive evidence why hiring is strong in this industry, but the assumption must be that most medical products companies are flush with cash, have products ready for launch in the next year, or are building staff in advance of an upswing in the economy. It could be all of the above. As discussed previously, the medical products industry is currently undervalued, especially if the predicted decrease in unemployment and improvement in the economy occurs late in 2010.
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Designing better medical products

I am an early adopter of any new technology, not only because I like new gadgets, but because I always expect the newer technology will have improved quality, power, and ease-of-use. Sometimes, I am quite pleased with the results, my iPhone from Apple being one of the better examples. More often than not, I find myself quite disappointed.

Without intending to be an uncritical fan of Apple (you can find those discussions in
several other locations on the web), there are real reasons that the iPhone is simply the best cell phone on the market. First, it holds a good sampling of my music collection, eliminating one other device to carry with me. And that music is transferred to my iPhone by simply the most elegant piece of software I’ve ever used: iTunes. I hear people tell me that they can get music on their phones, but it takes work. I have no time to figure out arcane programming steps to get music on some other device. The music simply gets onto my iPhone, I can access it. That’s the ballgame for me.

Second, I have downloaded and installed onto my iPhone dozens of
Apps, which are the programs for the iPhone. I have games, access to sports scores real time, business news, stock prices, maps, movies, Kindle books (this is a whole story in itself), and an amazing program that listens to music and identifies it (and it’s free). Using iTunes, I can buy the apps (many are free, but you still have to “purchase” them) at the iTunes store, and upload them to my iPhone. At its essence, iPhone has made my life easier. Read More...

New FDA Commissioner

On March 11, President Obama appointed Margaret A. Hamburg, MD to be the new FDA Commissioner. She has a substantial educational background including an MD degree from Harvard and training in neuropharmacology. She has had long public service at the U.S. Office of Disease Prevention and Health Promotion, the National Institute of Allergy and Infectious Diseases at NIH, where her work focused on AIDS research, and Health Commissioner for New York City. President Clinton selected her in 1997 to be assistant secretary for policy and evaluation at the U.S. Department of Health and Human Services. Not only does she have a background in healthcare policy, medical research, and the bureaucracy that controls both, she has experience with industry, sitting on the Board of Directors of Henry Schein. Read More...

Successful Marketing Management

I haven’t done an entry in about a week, because I have been focused on a consulting assignment on pricing strategies in a couple of medical device segments. Interestingly, it was for a large investment banking firm. In this down-market, research into medical companies, because they are spending more time analyzing the fundamentals of these corporations.

Part of my assignment was to give a one day training session on how manufactured products get to the market. Trying to condense 20 years of knowledge in this industry down to a six hour Powerpoint presentation (yes, too long, but they didn’t have 20 years to get up to speed) is challenging, but it was critical to their understanding of the medical products market.

I often relate a story about the medical products market whenever I am interviewing someone for a marketing position in this industry which helps define the almost every challenge for
product marketing managers in this business. There are over 50,000 medical products companies in the United States (probably more, but it’s hard to obtain exact data). If each one of those companies sent a sales representative into a physician’s office, surgery center or hospital, there would be no time for patients. Since the primary (but hardly exclusive) method for marketing a medical product is through the sales process–new product introductions are especially sales critical. Read More...

The recession and the medical industry

I have been in numerous positions within the pharmaceutical, biotechnology and medical device industries over the past 20 years. The one paradigm upon which we all relied during those years was very simple: “the medical industry was recession-proof.” In fact, way back in 2008, medical products stocks, including Big Pharma and medical device manufacturers, were considered safe locations to invest during a economic downturns. Industry analysts, executives, and investors believed that people would continue to buy medical services, who would then buy all of the products from table paper to expensive capital equipment.

Current speculation seems to reinforce the old paradigm. A
recent article published in Tech Journal South offers up the following optimistic forecasts:

  • M&A activity will increase significantly.
  • Biotech stocks will outperform the rest of the market (which shouldn’t be hard given the continued implosion of stock values)
  • Most investors consider biotech undervalued
  • Most expect biotech to rebound either this year or next
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Ethics and medical sales

While searching for information on another blog entry of mine, I came across a story where a Stryker sales representative in Ohio pled guilty to felony “misbranding of a medical device.” As an executive and manager in the medical device and pharmaceutical markets, my rules were quite explicit to all sales people--do not violate applicable regulations and laws for marketing medical product. Stryker has a similar statement on its website (though I cannot know if they placed it there after the criminal actions, but most ethical companies have the policy in place). Read More...