Proxima Clinical Research Unveils Accelerator Program – M1 MedTech

Clinical research organization also has plans to launch incubator as part of its initiative

HOUSTON--(BUSINESS WIRE)--Proxima Clinical Research, a contract research organization (CRO) based out of the Texas Medical Center, announced today its plans to launch its own accelerator program – M1 MedTech early next year. The company has raised funds for company launch and investment in several new companies as part of the initial cohort.

“Our goal is to move these companies substantially forward in a short amount of time,” said Kevin Coker, CEO of Proxima. “Proxima is in a unique position to leverage our experienced team of regulatory, quality, and clinical experts. We won’t be working at arm’s length from these companies. We will be a big part of what they do every day.”

M1 MedTech was created to support early-stage medical device companies, offering an immersive experience that provides tangible benefits to participating companies. The program will take on a limited number of companies in each cohort and offer a hands-on approach to helping founders advance their companies and technologies. The coaching process will include a curated educational program, interactive workshops where participants can continually build out specific company deliverables, and one-on-one mentoring.

“This will be a unique experience for all parties involved, as Proxima is also a young, yet established, company that is now creating a program to assist companies at an earlier stage,” said Larry Lawson, co-founder of Proxima. “Our experience in the CRO realm and ability to provide coaching in clinical, regulatory, quality, and go-to-market strategies will only strengthen M1 MedTech’s ability to support the success of emerging companies and provide more life-saving technology to the public.”

“M1 will be a place where startups can go to receive concrete resources to further their development. The participant success is our sole focus, and the ultimate goal is to have a substantial impact on the ideation-to-market process for Class II and Class III medical devices,” said Isabella Schmitt, director of regulatory affairs at Proxima and a principal at M1. “Proxima’s specific expertise alongside our M1 partners will provide resources for all key areas of a medical device entrepreneur’s journey to market and beyond.”

For now, M1 MedTech will function as an accelerator focused on more involved Class II and III medical devices. As the program continues to grow, the team plans to build out an even more extensive incubator focused solely on Class III devices.

“We don’t view M1 as competitive to other accelerators, rather we believe it will offer a different experience. Our team will strive to create a personalized program where companies have a dedicated touch point throughout the process,” said Sean Bittner, director of programs at M1 MedTech. “We will also provide specific, tailored connections and resources vetted by our team through professional partnerships, not just a general list of industry contacts.”

M1 MedTech plans to open applications in spring 2022. To learn more about Proxima CRO and M1 MedTech visit ProximaCRO.com or m1medtech.com.

About M1 MedTech

M1 MedTech is an alternative accelerator/incubator program designed to support and expedite the advancement of early-stage medical device companies. The program offers an immersive experience that provides tangible benefits to a limited number of participating companies, offering a hands-on approach to helping founders advance their companies and technologies. The coaching process includes a curated educational program with a focus on regulatory and quality dynamics and interactive workshops where participants can continually build out specific company deliverables, as well as one-on-one mentoring. The program was launched as part of an initiative by Proxima CRO, a contract research organization (CRO) based out of the Texas Medical Center, with the ultimate of substantially impact the ideation-to-market process for Class II and Class III medical devices.

Chelsi Smith
csmith@piercom.com
956-358-3300