Thank you for your interest in the Center for MedTech Excellence.
Background:
To be eligible for assistance, the following minimum criteria are required:
- Located(headquarters or other facilities)in the State of Georgia or the Southeastern United States (NC,SC, FL, MI, AL, GA, TN and VA).
- Plans to manufacture in Georgia.
- Product is FDA regulated, with an anticipated or defined regulatory pathway (class 1, class 2, etc.).
- High level or defined ‘go to market strategy’ exists, based on initial feasibility work and market assessment
- Anticipated commercialization of product within 2–3 years (or less)of application date.
Eligible applicants will follow the Center for MedTech Excellence application process including:
- Application Form
- Signed MNDA
- New applications will be reviewed at least monthly by a Mentor team consisting of representatives from the ATDC, GCMI, and GaMEP.
- Initial application responses will be provided within 45 days or less of the application date.
- All applicants will receive feedback from the Mentor team, who will determine whether:
- The Applicant meets the assistance criteria and will move to the next phase.
- The Applicant does not meet the criteria for assistance.
- The Mentor team will need additional information.
- The Applicant likely can meet the criteria for assistance but may require further pre-work and assistance from the Center to fully engage Center resources.
- If selected, a formal on-boarding process will be scheduled with the applicant and the applicant will be assigned a specialist who will guide them through the process.