Medical Devices Group

  • Community
  • Webinars
  • Jobs
  • Events
  • Contact
  • Go Premium
« Back to Previous Page
like 2 comments  share
Joe Hage
🔥 Find me at MedicalDevicesGroup.net 🔥
April 2013
Qualitative Marketing Research for Medical Devices
3 min reading time

medical-device-conference-Margie-FlaggPeople most often think of marketing research as those check-the-box surveys that crop up on the Internet. But qualitative research, based on a conversation with the respondent rather than a survey aimed at the respondent, can play a major role in various stages of a medical device’s marketing lifecycle.


Guest author Margie Flagg writes,

“When using qualitative research, you want to make the researcher as much a part of your team as possible. The researcher will be having an unbiased conversation with your target audience, that’s part of the research protocol. But, you want the researcher to be privy to your goals and as much technical information as you can share, so that the researcher can direct the conversation to areas that you find important. Having had client side experience and being a part of various launch teams has been very valuable to me as a researcher. I’ve lived through many of the issues that are faced during a product launch.

During the development stage, qualitative research can determine the largest unmet needs in a particular area. That input can be used to develop a new device or fine tune the development of a device in process. With various websharing programs, these interviews can be conducted on the phone. Using phone interviews, thought leaders or healthcare professionals at the type of institutions that the marketer wishes to target are readily accessible.

Once the device has been developed, there are a variety of studies that enhance the launch process. Device usability, an item that the FDA now includes in its evaluation of a new device, can be conducted using face-to-face interviews at facilities in most major cities in the US and Europe. Marketers can see how respondents would use their devices in simulations. This approach highlights potential training needs and refinement in packaging and presentation during use. If your audience is a small specialty with wide geographic dispersion, conventions are often a cost-effective route to finding enough respondents in one place to obtain reactions.

The need for training, the amount of training required, and the best vehicles for training are also topics for qualitative research. Talking to actual potential users and testing proposed training mechanisms can bring to light issues that developers, because they have been so intimately involved in the product, never thought of. Better to iron out the kinks ahead of launch then to have to deal with them after.

Patient information is another area where qualitative research can provide the developer with insights as to how patients would interpret your instructions and how best to construct those instructions to meet FDA guidelines.

Of course, once your device is launched, follow-up research with users, discontinuers, and those aware of but who haven’t tried your product will allow you to keep your marketing plans on track. In a nutshell, that’s the goal of qualitative research—to provide you with nuanced, actionable information to keep you and your team on track for a successful product lifecycle.”

About the Author: Margie Flagg will be sharing her insights at the 10x Medical Device Conference next week. She is the owner of Market Research, PRN. She has more than 25 years’ experience in medical devices and pharmaceutical marketing research. She is an experienced qualitative and quantitative market researcher, with broad experience in the medical device field. With both client side and vendor side experience, Margie can provide you with insightful answers to your questions and flexible research options.


Sherry Ling
LinkedIn.com/in/sherrylingx
Sherry.B.Ling@gmail.com
After being in pharmaceuticals for many years, I did not realize that bringing a medical device to market involved getting FDA approval for verbiage surrounding how patients would interpret the instructions and how to best construct those instructions. In essence, market research is collected using patient focus groups and gathering information on patient interpretation of instructions for usage of the device.

This was a wonderful article and very informative. Thank you!

Jose M. Montero
josem.montero@gmail.com
IMHO one aspect many times overseen or simply ignored is the appropriate translation into target country languages of these (and some other) materials. The range of professionals you can reach to with an accurate and professional-made translation is wider and the level of awareness and implication you get from the doctors and healthcare people is greater. At least that’s my experience as a medical translator into Spanish.
On the other hand, the article is quite well structured and points out several important factor to be considered.

Marked as spam
Posted by Joe Hage
Asked on April 12, 2013 1:04 am
399 views
  • Follow
  • Unfollow
  • Report spam
like 2 comments  share

Meet your next client here. Join our medical devices group community.

« Back to Previous Page
Ask a Question
Leave a Comment

We still use LinkedIn to access our site because it’s the only way to “pull in” your LinkedIn photo, name, and hyperlink to your profile page, all vital in building your professional network. When you log in using LinkedIn, you are giving LinkedIn your password, not me. I never see nor store your LinkedIn credentials.

Stay connected with us.

By signing up you are agreeing to our Privacy Policy.

Categories

  • Capital/Investment
    • Business Model
    • Funding
  • Careers
  • Design/Devel
    • Design
    • Development
    • Human Factors
    • Labeling
    • Material Selection
    • R&D
    • Trials and Post-Market
  • Featured
  • Industry
    • Announcements
    • Device Tax
    • Hospital and Health Care
    • Innovation
    • Medtech
  • LinkedIn, etc.
  • Markets
    • Africa
    • Americas
    • Asia
    • Australia
    • Europe
  • Regulating
    • CE Marking
    • EU
    • FDA
    • FDA/EU etc.
    • Notified Bodies
    • Quality
    • Regulatory
  • Selling
    • Distribution
    • Intellectual Property
    • Marketing/Sales
    • Reimbursement
  • Worth bookmarking!
Feature your job here.
logo

Companion to LinkedIn's 350,000 member community

  • Contact
  • Medical Device Marketing
  • In Memoriam
  • Medical Device Conference

The Medical Devices Group   |   Copyright © 2025 Terms, Conditions & Privacy

Medical Devices Group
Powered by  GDPR Cookie Compliance
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.

Strictly Necessary Cookies

Strictly Necessary Cookie should be enabled at all times so that we can save your preferences for cookie settings.

If you disable this cookie, we will not be able to save your preferences. This means that every time you visit this website you will need to enable or disable cookies again.