Innovate with Confidence
At Bold Type, developing medical device apps is all we do. And when you do one thing over and over, you get very good at it. Our leadership team has decades of experience developing sophisticated, secure software solutions for regulated markets. We’ve used that experience to reimagine how medical device apps are developed. As a result, we can develop a medical device app for you that is secure, FDA-compliant, beautiful, and functional. And we’ll do it faster than anyone out there and at a cost that will surprise you.
Pioneers
Who We Are
We are pioneers in the development of medical device apps, specializing in creating secure, compliant, and user-friendly software solutions.
Our expertise spans usability, regulatory and cybersecurity, ensuring that your medical device apps meet the highest standards.
Our Unique Offering
What sets us apart is our innovative medical device app platform, designed to rapidly develop iOS and Android apps that seamlessly connect wirelessly to medical devices and the cloud.
This allows us to deliver
And we don’t just deliver the app.
We deliver the full documentation package that fits into your product’s design history file (DHF) to ensure and support FDA compliance.
Exceptional Team
Powering Our Company
Jose founded Bold Type to help companies solve hard technical problems. He has more than a decade of experience as a technical contributor and executive in various industries. These include the semiconductor industry, medical devices, consumer electronics, health and fitness, and the Internet of Things. Jose completed his PhD in electrical engineering and computer science at MIT with a minor in business administration from the Sloan School of Management.
Jose Bohorquez / PhD
President
Mohamad has more than 25 years of leadership experience developing secure software for mission-critical applications. His leadership experience ranges from CTO at a medical devices startup to Chief Software Architect at a Fortune 500 company. He has led hundreds of software projects ranging from embedded drivers in tiny microcontrollers to global enterprise and government communication systems with the highest levels of security. Mohamad designed and implemented the first and only in-browser crypto module to receive FIPS 140-2 certification and the only FIPS 140-3 compliant solution for securing commercial devices in classified spaces. He has worked directly with the highest security organizations in the US (NSA, CIA, DISA, DoD) to develop highly secure communication systems, and he designed one of the only software systems in the world that can thwart both Spectre and Meltdown attacks per NSA’s review. As a partner and Chief Software Architect at Bold Type, Mohamad now dedicates his vast software and cybersecurity expertise to helping medical device companies bring secure, FDA-compliant software to market. Mohamad received a Bachelor of Engineering degree from Imperial College, London, and has a Master’s Degree in Computer Science, completing all coursework required for a PhD with a 4.0 GPA.
Mohamad Foustok, / PhD, ABD
Chief Software Architect
Andres has over 15 years of experience across the full cycle of product development from product strategy to R&D to product launch. His career has allowed him to work in multiple industries ranging from power generation to aviation and IT. He has launched over a dozen products, stood up product development processes and organizations in startups, growth stage, and large firms. Along the way, he has gotten to collaborate with some of the best people the world can offer in strategy, innovation management, change management, and organizational design. Most recently, Andres served as VP of the Information Systems and Services division of a growth-stage defense technology firm. There, he developed and launched products in the enterprise asset and health management space and developed a data science and big data analytics portfolio of services. Andres has a Bachelor's degree from the University of Florida and a Master's degree from Harvard University.
Andres Echeverry / VP
Product Development
Jackie has more than a decade of experience in medical quality assurance and regulatory affairs. She is an expert on FDA Traditional and Special 510(k) submissions, with more than twenty 510(k) clearances under her belt. These include diagnostic, implantable, disposable, and reusable medical devices. She also has experience with European Union (EU) Technical Documentation along with Canada, Japan, Australia, South Korea, Middle East, and Singapore submission experience. Jackie is also well versed in Internal and External Auditing for US FDA and EU Notified Body. Jackie holds a Bachelor’s in Biology and a Master’s in Regulatory Affairs.