• Cybersecurity Specialist: product security is a key challenge to medical device software, given the continuous threat of data corruption and product hijacking. As hackers get smarter with their strategies, the industry desperately relies on third-party services to help them stay one step ahead and ensure that their products are rigorously secure from external threats.
• Third-Party Software Developers: with the demand for software development often outweighing the capacity of the team, the industry relies on the expertise of third-party software developers to ensure their products enter the market in a timely and costly manner.

• Verification, Inspection, and Testing Services: the high cost associated with compiling the necessary data and information for regulatory body submission creates a high demand for external expertise in post-market surveillance, risk management, diagnostic, V&V, interoperability, and reliability testing.

• Regulatory and Quality Consultants: in an ever-evolving regulatory landscape, medical device developers are actively seeking out regulatory and quality consultants to function as a sounding board. Developers rely on their expertise to ensure their products consistently align with new regulations, standards, and guidelines so that they can continue to create innovative, compliant, and competitive devices.

If you offer any of these services, collaborate with us to create a bespoke partnership package that aligns with your preferences, ensuring you connect with the individuals you want, in the matter that suits you best. Whether through presentations, one-on-one meetings, booths, private dinners, take advantage of this opportunity to spotlight your solutions and achieve your business development objectives.