Where are they now? Our 2019 deep-dive Q&A with SweetBio CEO & Co-founder Kayla Rodriguez Graff

Three years, two rounds and one ‘market reprioritization later,’ SweetBio is poised to enter the $10 billion wound care market this year. While FDA work continues on a first in kind pre-implant dental application of its Manuka honey and collagen derivative membrane product Apis, the company has pivoted to a planned, but previously secondary market. Why? A faster regulatory pathway and larger addressable market.

SweetBio Co-founder and CEO Kayla Rodriguez Graff was kind enough to share nearly an hour with Write2Market VP of Healthcare Paul Snyder. They talked about the company’s progression, ‘market reprioritization,’ learnings and more in the nearly four years since we first featured them following SEMDA 2015.

Kayla Rodriguez, MBA – Co-founder & COO, SweetBio

Paul: “What drove your reprioritization from a first in kind dental implant regenerative product to wound care in general?”

Kayla: “Our baseline technology, which we call MXTECH, is a true platform. While the first manifestation of MXTECH was a regenerative membrane for dentistry, we quickly discovered the direct translatability and extreme market demand in adjacent markets, including wound care. As honey has never been cleared for use in dental, the regulatory pathway became more difficult. Because we had already examined the wound care market and heard from early customer discovery that our product is ‘exactly what they have been looking for,’ we were confident in this pivot.

“We were grateful to be working with world renowned wound care clinicians, including Dr. Lillian Nanney and Dr. Jeffrey Davidson at Vanderbilt University, who provided incredible feedback as we prepared for the wound care industry. Because of the background work completed on the safety and efficacy of MXTECH, and because there are currently over a dozen Manuka honey wound care products commercially available, we were able to translate our dental regulatory documentation into over a 1,000 page wound care 510K application in just 40 days. We expect to our first product to enter the $10 billion wound care market – with solid, existing reimbursement opportunities in place – this year.”

Paul: “SweetBio recently closed a new funding round. What messages resonated most with your investors?”

Kayla: “A $10 billion market and an investable opportunity with high growth return potential. There is also strength in our multiple bottom line message. We are able to demonstrate a proven record of delivering on dollars received including spending plans, accountability, clear messages and consistent communication with our investors. We are an investable company with high growth potential and a diverse, woman-led company.  

“Because we stand for better healing, everyone has a relatable story, which usually involves witnessing a painful healing experience with an aging loved one or even a beloved pet. We are also tackling a problem with an on-trend natural solution without having to sacrifice performance for ingredients.”

Paul: “What have you learned about the FDA process that could be useful to very early stage innovators – like yourselves three years ago?”

Kayla: “First, understand your claims and pathway. Word choice is monumentally important. Just one or two words in your claims can push a 510k to a PMA. Next, find the right partner, especially regulatory consultants that are experienced in your product class and FDA branch to communicate that word choice. Then, finalize your product design in a way that enables you to manufacture at scale with economics that make sense. The last thing you want to learn is that you have $100 product COGS that can only retail for $20.

Paul: “What would you do differently?”

Kayla: “Hire full-time, high quality consultants up front. Pay them to work every day as early as possible with complete focus on, and enthusiasm for, what you are doing. Conversely, move faster on removing bad partners. They might not be bad people, but if they are misaligned with your vision, remove them swiftly.”

Paul: “What makes clinicians (potential customers) more likely to engage with a pre-FDA healthcare startup?”

Kayla: “Referrals are the way we get early interest from clinicians. We don’t succeed at cold calling. Even clinicians follow the common diffusion of innovation curve – people are either innovators, early adopters, in the majority or laggards. Understand your value proposition for each group, then find early adopters willing to try something different and are excited about it. The value proposition and strategic alignment with innovators or early adopters lies in an existing interest in innovation and industry leadership, which includes being part of the research and publishing.

Paul: “How did you get to be part of Prudential’s ‘State of Us’ commercial happen?”

Kayla: “That was absolutely amazing. Their own team picked cities with statistics that drove unique financial decisions. They picked Memphis due to its massive increase in the number of  women owned businesses. We had no contact with them prior to being asked to participate. I believe that our visibility in the entrepreneurial and life sciences ecosystems, serving on boards including Epicenter and New Memphis Institute, participating in community activities as mentors, our mission and diversity helped them find us. After eight rounds of interviews, we got the gig!

Paul: “What’s the lesson there?”

Kayla: “When you serve, good things happens. What happens outside of your office or lab is equally as important as what happens inside of it. You won’t see immediate results. Do it from a different place, a place of service. In our case, our commitment to our community and service ultimately helped raise money, connect to clinicians, gain access to more boards and other resources like our new office at the University of Memphis CommuniTech Research Park initiative.”

Paul: “What has been most surprising about your journey to date?”

Kayla: “How my role has changed. Each day, I focus on identifying the right work that aligns with strategic objectives and putting the right people on that right work. It has shifted from putting processes in place for projects with more partners and help the business run more efficiently. Axel Strombergsson, our new chief operating officer, was built for that. With Axel on operations and myself on the future activities of the company, it frees up our co-founder and Chief Science Officer, Dr. Isaac Rodriguez, to soar at his strengths – reinforcing the scientific credibility of SweetBio. The culture of our company is strong and I am proud of it – we each have the opportunity to soar at our strengths while we drive incredible progress for the company.

“We plan on doubling our team in next 12 months while ensuring we’re operating in a way that’s energizing. I’ve been spending and enjoying more time focusing on the team and our culture – different and surprising for me – and I’m highly energized by it.”

Paul: “What do you need next?”

Kayla: “Two things. First, interview around 100 wound care experts for customer discovery. Second, identify and learn from business mentors who have done what we are hoping to do: to build, launch and scale a company both nationwide and globally.”

Paul: “What are you interested in learning from the collective ‘medtech’ community?”

Kayla: “The New Memphis Institute, a community leading nonprofit in Memphis, does a ‘speed mentoring’ event. I’m interested in more one-on-one knowledge sharing from the Randy Scotts and Bob Crutchfields of the world in a low-risk environment. There are always questions about reimbursement, resource recommendations and what are the top questions to ask distributors in contracts? Having access to mentoring from these inspirational leaders can be company altering for a scale-up company.”

Follow SweetBio on LinkedInTwitter and Facebook.

Unpacking the latest in blockchain for healthcare with Florence Hudson

“It isn’t about greed, it’s about quickly and securely sharing data to improve health outcomes.”

Florence Hudson

Blockchain, or, more generically, “digital ledger technology” is going to impact a very large, highly educated army of doctors and clinicians, IT professionals, cybersecurity specialists, organizational leadership, federal regulators, patients and more.

“Ultimately, blockchain for healthcare isn’t about greed, it’s about quickly and securely sharing data to provide valuable content and context to improve outcomes,” says Florence Hudson, a former IBM vice president and chief technology officer and current founder and CEO of advanced technology consultancy FDHint, LLC.

But the sharing of data without a centralized authority (digital ledger technology) brings security and provenance questions that haven’t been answered. Yet. In advance of her SEMDA 2019 Medtech Conference keynote which intends to unpack the current state, goals and opportunities for digital ledger technology in healthcare, Ms. Hudson shared with us the following.

Q: How would a seed stage investor begin to evaluate a healthcare blockchain startup?

A: The investors will need to engage a technologist to examine the startups’ technical risk. What is the true immutability of the company’s offering? Are they creating a central authority or are the data truly distributed? Do not be wowed by the blockchain. It must work in a significantly different way in healthcare than in the financial system.

If a young company is espousing a valuable blockchain for healthcare technology, they must be able to convincingly answer how they have architected and enabled TIPPSS – trust, identity, privacy, protection, safety and security. How are they entrusting that it is actually the doctor accessing an implanted, data-generating device and the ledger? Is that doctor still with the same institution? Are they still credentialed for example? Satisfying TIPPSS is a LOT to achieve, so beware and engage experts for evaluation.

Q: How do buyers in this technology evaluate its potential or utility?

A: What is the technology’s value proposition? Can it ensure data provenance without a central authority? Let’s look at sample data tracking of biomarkers for cancer care. Labs, patients, hospitals and providers, CROs, payers and regulators will all need to access and understand how a distributed ledger technology benefits them. Is it financial, risk reducing, efficiency generating? Will you be able to track those data and process them more easily? That could be a powerful value proposition.

Q: Where are the top immediate needs and potential startup opportunities for blockchain in healthcare?

A: Secure data sharing via blockchain moving us toward precision medicine and precision oncology, blockchain for the pharmaceutical supply chain, as well as blockchain for clinical trials are at or near the top of the list. In a clinical trials scenario, imagine a distributed ledger that could synchronize a pharmaceutical manufacturer’s clinical trial development process with regulators and providers, then connect to a public blockchain for patient advocate groups to increase the number of participants in the trial. The manufacturer of course wouldn’t share proprietary details of the chemical compound(s), but it may more effectively make the trial and benefits known to the concerned community. If we can streamline the clinical trial process, we could accelerate drugs to market and improve healthcare outcomes.

There are clear opportunities for hospitals and connected devices, data sharing for precision medicine and personal patient medical records. If you could securely acquire data from a contextual history (i.e. multiple family members), connect with permissions to them, then connect to those with similar DNA, who knows what we could do?

Ms. Hudson will unpack all of this further and dive into important issues not addressed here, like IEEE prestandards work for clinical IoMT and data in blockchain, existing partnerships and deployments and more in a keynote at the SEMDA 2019 Medtech Conference April 8-10 in Atlanta. Register today!

How big of a bite can AI take out of health insurance fraud?

A health tech startup born at Georgia Tech may end “pay and chase” for health insurers’ special investigations units.

Healthcare fraud in the United States is estimated to cost the system $270 billion every year. Scams are constantly evolving. Current detection techniques and whistleblowers only uncover a small fraction of this.

Dr. Musheer Ahmed

Founded in March 2017, FraudScope is the brainchild of Georgia Tech alum Musheer Ahmed, Ph.D. The company’s AI-based SaaS platform origins can be found in Dr. Ahmed’s dissertation on applying cybersecurity concepts in healthcare. Fraudscope is commercializing the patented AI-based technology to detect fraud, waste and abuse (FWA) in health insurance claims data from his dissertation.

“Every health plan has a special investigations unit (SIU) to identify FWA in health insurance claims,” says Dr. Ahmed,FraudScope CEO, CTO and Founder. “When plans receive a claim for payment, they have a limited number of days to make that payment. If initial, simple checks for validity discover nothing suspicious, they pay the claims and then further examine for anything potentially fraudulent, wasteful or abusive. If this further examination uncovers patterns of FWA within paid claims, insurers have to chase the money for recovery which is difficult and costly to attain.”

How then do you optimize the use of limited special investigation unit resources to maximize savings?

FraudScope brings sophisticated AI-based technology currently absent in the FWA detection realm for insurers to identify those claims before payments are made. And because the machine learning capabilities aren’t rules-based like most existing solutions it can adapt to new scams at very high speed with low false-positive rates. The days of playing ‘pay and chase’ for insurers, their audit teams and special investigations units may be nearing an end.

Dr. Ahmed says that every health insurance plan that has seen a demo of FraudScope has signed on to pilot the technology. FraudScope’s pilots have identified a significant amount of claims containing FWA that were paid at those plans. The company’s target market is currently commercial payers, though they will target public payers such as CMS and the VA in the future as well.

Patrick Stamm

FraudScope announced a $1.5 million seed fund round shortly after its founding in April 2017. Among the investors and now principal advisor to FraudScope are former UnitedHealthcare COO of Shared Services Patrick Stamm. The company plans another funding round later this year to expand its sales and engineering teams. The goal: acquire more customers and rollout additional products such as pharmacy/drug claims and workers compensation FWA detection.

When asked what FraudScope needs from the southeast medtech community, Dr. Ahmed said, “More interactions with health insurance plans to make them aware of what we can do, especially SIU directors, audit teams and payment integrity officials at health plans.”  

When asked what advice he would share with other innovators or engineers who believe they may have a technology ripe for commercial development, Dr. Ahmed said, “Because there is so much potential for improvement in healthcare, connect with foundations and apply for commercialization grants. Healthcare innovation, including the insurance space, moves more slowly than almost any other industry. Be prepared for a longer sales timeline than you might anticipate.

“There is a great deal of lot of support in the Atlanta local and regional startup ecosystem. The ecosystem has matured significantly in the past few years. Young companies should be confident that there is sufficient local and regional support for their journey without needing to court Silicon Valley.”

Connect with the entirety of the Southeast Medtech Ecosystem at the 2018 SEMDA Medtech Conference May 2-4, 2018 in Greenville, SC!

Patientory expands their network and wins 10k during SEMDA 2017

Without a doubt, one of our favorite aspects of the SEMDA conference is meeting scores of young, investible companies that attend and pitch to the whole of the Southeastern medical device ecosystem. On day two of the conference, five startups pitched their companies reinforcing the strength of the technologies coming out of the Southeast. Congratulations to each of our PitchRounds finalists Myolyn, SweetBio, Patientory, Demore MUSC, and Contego Medical. The competition was exceptionally tight but at the end of the day, Patientory claimed the top prize.

Accepted as the first healthcare transformer in Boomtown’s Healthcare Accelerator, in partnership with Colorado Permanente Medical Group, Patientory is the first and only distributed blockchain cybersecurity technology for healthcare. They combine the power of rapid and secure medical record access with a patient community platform to reduce healthcare data breach and provide a centralized patient record depository- connecting the provider with the entire patient history to enable better chronic care management.

As we all know, patient history storage is fragmented. Each healthcare provider has their own Electronic Medical Record (EMR) vendor and platform. Those systems do not speak to other hospitals, practices, or specialists making it difficult for all parties to achieve care coordination. Patientory changes that by utilizing blockchain technology.

Patientory CEO, Chrissa McFarlane, recently shared with us a few insights about the company’s SEMDA 2017 experience.

What was your experience at SEMDA 2017 like?

“SEMDA proved to be a very worthwhile experience. Not only did our team feel a real sense of validation upon winning the SEMDA PitchRounds $10K cash prize and invitation to attend AdvaMed 2017, we were able to meet many industry leaders and investors which made our time at the conference an experience of high value. Let me say, it was an overwhelmingly positive experience.

I have presented our company during multiple pitch competitions but SEMDA was by far the most healthcare focused I have experienced. It was amazing to explain Patientory’s solution without needing to explain the current state of healthcare or the dated standard of EMR keeping. And because SEMDA is THE place for medtech leaders in the SE, I received quality feedback from industry mavens that are well versed in the space- SEMDA was a valuable experience for our team.”  

What were the results?

“Everyone I spoke to following the PitchRounds and throughout the entire conference were savvy healthcare leaders who could see right off the bat that we were meeting a real need. We had meetings with multiple investors and vendors during SEMDA- and the connections we made during those two days are continuing to evolve.”

What advice would you give medtech startups considering attending?

“Definitely utilize the resources provided by SEMDA and take full advantage of the annual conference as a place to meet vendors and potential partners. SEMDA is a great networking opportunity and by far the premier medtech event in the Southeast. I know SEMDA is an event that we will continually attend in the years to come.”

The company recently announced a raise of $7.2 million in an “initial coin offering” crowd sale. WOW! Driven by 1,728 investors, the company reached it’s funding goal in three short days- changing the game and utilizing an innovative funding model. The funds raised will be used to officially launch the Patientory platform.

Congratulations and thank you, Chrissa! We can’t wait to see Patientory grow and what you will have in store for us at SEMDA 2018 and beyond!

We are already counting down the days until SEMDA 2018 in Greenville, SC. In the meantime, follow SEMDA on LinkedIn and Twitter to stay up to date with the latest southeastern medtech news and events like our Medtech Women@SEMDA conference.

How SEMDA delivers value for our partners: Q&A with MMA’s Courtney Warren

At SEMDA, our industry partners and sponsors are the ones that make it possible to advance our collective mission: accelerating device development and achieve commercial success with access to funding, education, and networking opportunities for medical device companies, inventors, physicians, investors, tech transfer offices, universities, sponsors, and service providers interested in growing the medical device industry in the Southeast.

We know we also have an obligation to provide value to our partners. Courtney Warren, consultant for the Marsh & McLennan Agency shared with us how SEMDA meets that obligation.

Courtney Warren

How does SEMDA drive value for your investment?

“Our mission at Marsh & McLennan Agency (MMA) is to help clients by delivering smarter, local knowledge and world class solutions in employee benefits and risk management. Our partnership with SEMDA allows us to engage with the entire Southeastern medtech and medical device ecosystem. As such, we gain a better understanding of industry issues.  We have the opportunity to give back to the community through leadership, making us better equipped to connect clients with valuable contacts – capital investors, suppliers, or other business partners. SEMDA provides key connections and resources to bring innovation to market.”

What have the results been related to your SEMDA investment?

“SEMDA serves as the central connecting hub for the Southeast medtech community. We have met new companies at SEMDA that are now MMA clients. Through our involvement with SEMDA, we have been able to connect our clients with investors, suppliers, and specialists to help their business succeed.”  

What’s most needed in the Southeast medtech and medical device ecosystem?

“Industry advancement happens in small groups. Beyond the annual conference, we need vehicles that foster more in-depth conversations. Every member of the ecosystem offers a unique perspective, which we would like the opportunity to learn about in order to innovate our business strategy for our clients and the community.  Our work with companies developing medical devices and technologies is enhanced by input from CPAs, legal, and regulatory consultants.

“Knowing the right time to pull each other into the mix is a high-value proposition to ensure the best use of scarce resources. The better we know each other and our unique talents, the faster the right person will come to mind when we need help to advance our business and our clients’ objectives.”

If you would like to know more about how SEMDA drives value for our partners, email Executive Director Jason Rupp – jrupp@semda.net

Access the entirety of the Southeast medtech ecosystem in a ‘one stop shop’ at SEMDA 2017, April 26 & 27 in Atlanta.

How SEMDA helped create a company preventing “accidental addicts.”


Ashley Hancock, COO, Founder & Director of Intent Solutions

Depending upon your study of choice, medication non-adherence creates between $100 and $400 billion in wasted U.S. healthcare spending every single year. Yes, pill bottles have a child-proof lid, but that does nothing to make adults accountable when dosing medication or taking it on time. What about people who think two pills are better than one? That’s not always the case with regards to medicine, and that is almost always a step into the pitfall of addiction.

Intent SolutionsTM created a solution to help improve medication adherence and also to combat the notion that more is better when medicating. Their principal device is TADTM— “Take As Directed.” It is a smart medication dispensing device that is designed to markedly improve the monitoring and management of medication adherence.

“TADTM was born from the idea that we could invent a technology that would help people take their medicine as directed to prevent misuse, abuse, and addiction,” says Ashley Hancock, Co-founder and COO of Intent Solutions. “With this device we are tackling the broad spectrum of non-adherence as well as the misuse of prescription drugs: a market that encapsulates more than $300 billion, $72 billion of which is attributable to direct abuse or misuse.”

TAD “Take As Directed”

Hancock is a long time supporter of SEMDA. His involvement spans 10 years including service as the Executive Director from 2011 to 2013. The story of Intent SolutionsTM begins at the SEMDA conference and develops through the ongoing engagement with the experts and resources that make SEMDA a ‘must go to’ conference year after year.

Preventing the next “accidental addict”
After overcoming an addiction to prescription pain medication following a severe hip injury, Martin Mclean, Director and Co-Founder of Intent, teamed up with entrepreneurs whose relationships can be traced to SEMDA: Dr. Van Crisco and Ashley Hancock.  Later, Sam Zamarripa and Lou Malice, a SEMDA regular, joined the team.

“Intent’s existence is directly attributable to our relationship with SEMDA,” Hancock acknowledges. “We continue to leverage the connections made through the conference: from relationships with seasoned advisors to the people we will contact for future investment.”

Today Intent is a company that might be able to prevent the next “accidental addict” and take a bite out of hundreds of billions of dollars in wasted healthcare spending.

“The Conference is a must-go in my opinion,” says Hancock. “SEMDA holds a wealth and depth of medtech and medical device industry knowledge. When creating a med-tech company you need advisors, consultants, and fund raisers. The conference makes it possible for an innovator to make connections with these individuals that they would not be able to make in a single event elsewhere in the region, if not the nation.”

Intent finalized a $1.5 million seed round in November 2016 and is eyeing a Series A in 2017. In addition to the current inclusion of Intent Solutions’ TADTM adherence product within an NIH study at Johns Hopkins University, Hancock says an announcement involving a study with another leading university hospital involving TADTM is eminent.

Advice from Ashley Hancock on how to make the most of SEMDA as a newly formed medical device company

  • Take advantage of the partnering platform: understand who is a part of SEMDA and how you can meet them.
  • Attend and pay attention during the educational programs. The panelists can become great resources for connectivity, consulting, and ultimately partnering relationships.
  • As a startup you never have enough money, bandwidth, or people so once you attend SEMDA, leverage your new connections to create future success.

“Some go to the conference just for the investor forum, and some go for the educational track; we go for both,” says Hancock. “It gives you access to the advisors and consultants that may even some day be a part of your team.”

SweetBio uses SEMDA as springboard to medical device startup growth

Kayla Rodriguez, MBA – Co-founder & COO, SweetBio

Three weeks before SEMDA 2015, SweetBio wasn’t even incorporated. Six months later, Innova and MB Venture Partners co-led a $900,000 seed round to support FDA 510(k) clearance and commercialization of the company’s Guided Tissue Regeneration Membrane (GTR).

A graduate of ZeroTo510, listed among TechCrunch’s Top 20 U.S. Accelerators, SweetBio has created a patent-pending dissolvable membrane that uses honey to encourage healing and produce better outcomes. While currently used in hospitals to treat ulcers and burns, SweetBio is the first company to leverage this naturally antibacterial and wound-healing ingredient in oral procedures.

SweetBio COO Kayla Rodriguez recently shared with us a few insights about the company’s SEMDA 2015 experience and plans for SEMDA 2016.

Why did you decide to invest in SEMDA 2015?

“A few weeks before SEMDA 2015, I was in San Francisco and we hadn’t even settled on a name for the company. When we heard about SEMDA, we realized it would be the perfect opportunity to determine if our pitch, our business model and our value proposition are worth something.

“In less than 3 weeks, we incorporated the company, put our first investor pitch deck together, practiced, practiced and practiced some more to get ready for PtichRounds.”

What was your experience at SEMDA 2015 like?

“It was the most wonderful experience. Gaining insights and feedback from David Huizenga, Chris Hooper, Randy Scott and others helped shape our company. They also introduced us to dozens of colleagues including other investors that have been instrumental in SweetBio’s growth. Having the undivided attention of seasoned medtech investors in a low-risk environment is something I had never experienced before attending the SEMDA conference in 2015.”

What were the results?

“We got to know more about who we are as a team. And while we don’t have all the answers, we have the grit and grind. Our experience at SEMDA 2015 helped refine our strategic direction, improved our pitch, opened new doors and helped validated our business.”

What advice would you give medtech startups considering attending?

“If you are not planning on pitching, no matter how early or young your company or idea, get it ready and just go pitch. Do whatever you can to take steps forward. Redefine winning. Winning PitchRounds is not all about coming in first. Winning PitchRounds is also in relationship building. Allow yourself to be social, be bold. The collective crew at SEMDA is most welcoming.”

What are your goals for SEMDA 2016?

“We are participating in PitchRounds again and we are treating it as a benchmark. We are proud of our progress, and this is a perfect opportunity to do a ‘temperature check.’ Having just celebrated our first year as a company we need to ensure we are focused on what’s critical to our continued development: de-risking our marketing plan and de-risking our trials plan.”

“We hope the investors will challenge us and poke holes in our pitch, so that in year two we focus on initiatives that continue to add value – especially to our go-to-market strategy.”

Thank you, Kayla! We can’t wait to see you and what you have in store for us at SEMDA 2016 and beyond!

Applications for PitchRounds at SEMDA 2016 open through May 2, 2016

PitchRounds and its corresponding online platform connect medical device startup companies with venture capitalists and angel investors who are seeking new investments. If you have a medical device or health IT company and you’re looking for venture funding, PitchRounds is for you.

Q&A with MB Venture Partners: What makes a young medtech company investable and why SEMDA 2016?

A few weeks ago we had the opportunity to speak with Gary Stevenson, co-founder and managing partner with Memphis-based MB Venture Partners. As we wrote recently, in late 2015, MB Ventures co-led a $900,000 investment in SEMDA 2015 alumnus SweetBio.

From his official bio: “Gary co-founded MB Venture Partners in 2001 after six years in healthcare investment banking and research. He also spent seven years in a variety of general management roles with Abbott Laboratories, one of the largest and most diversified healthcare companies in the world. Gary is a board member or observer for several MBVP portfolio companies including AxioMed Spine, BioSET, Kereos, KFx Medical, Hapten Sciences, S2 Interactive, Visioneering, Focal Point Pharmaceuticals, iScreen, Restore Medical Solutions, MB Innovations, EcoSurg, View Medical, Better Walk, Camplex, and CrossRoads. Gary also serves on the board of Life Science Tennessee and ZeroTo510.”

We couldn’t resist sharing Gary’s insights related to what makes a young medtech company investable and why the SEMDA annual conference is worth attending.

Q:  What is your investment “sweet spot”?

A:  MB Venture Partners began making investments in start-ups in 2002. We have invested in almost 50 start-ups since then. We focus mostly on medical device opportunities, but occasionally invest in biotech companies. Our preferred niche is musculoskeletal disease where we have special domain expertise and relationships. Two of the Memphis-based musculoskeletal companies are investors in our Funds. We have been hosting the investor-focused Musculoskeletal New Ventures Conference in Memphis now for 13 years in which SEMDA is a co–sponsor.

We deliberately diversify across stage, investing in some startups at seed and early stages while adding others that are in later stages of development. We have invested as little as $25,000 and as much as $5 million in our portfolio companies. Though most of our portfolio companies are in Tennessee, we invest all over the country with investments in San Diego and in Connecticut, for example. Lastly, we are active investors. We hold board seats in all but a very few of our portfolio companies.

Q:  How does the SEMDA annual conference demonstrate the greatest value for you?

A:  Over the years, several of our portfolio companies have attended and presented at SEMDA.  We are always eager to see the new and emerging technologies presented, looking for ones that might be the right fit for MB Venture Partners. We also enjoy networking with other investors who attend SEMDA.

Isaac Rodriguez, PhD, Co-Founder, CEO/CSO SweetBio

Q:  What stood out about SweetBio that other young medtech companies can learn from?

A:  There are several qualities about SweetBio that were attractive to us. In fact, many of those are qualities we have seen before in some of our most successful investments. SweetBio is focused on an unmet market need that looks to be large and growing. The team has the right mix of complementary and overlapping skill sets that inspires our confidence on execution. We like the current intellectual property position and the regulatory path seems straightforward.  

These are many of the same qualities we saw when we made our initial investment in Nashville-based BioMimetic Therapeutics in May 2003, an investment that turned out really well for MB Venture Partners. On top of all this, we really like the local connection for SweetBio. The team was part of ZeroTo510, a Memphis-based accelerator and performed very well. So for all these reasons, SweetBio stood out from all the other investment opportunities we looked at last year.

Q:  What would you tell other investors who might consider SEMDA 2016 about why it is worth their time to attend?

A:  There are many conferences that compete for limited investor attention. SEMDA is perhaps the most relevant in our region to those of us committed to the medical device industry. We hope to see many of our investor colleagues at SEMDA 2016.

Thank you, Gary! We look forward to seeing you in Nashville next month!

Investors, are you ready to find your next medtech investment? Or are you a young medtech company seeking funding and wondering who is going to pay for your innovation? SEMDA 2016 is the place for you.

Sincerely,
Jason
Jason Rupp, Executive Director, Southeastern Medical Device Association