The US Government critically needs breakthrough products with stable supply chains during times of crisis. Universities, research institutes and corporations struggle to translate advanced technologies to market. Triple Ring bridges the gap between the latest technological advances and products that solve real-world problems. By teaming with leading research organizations on government contracts, Triple Ring has established itself as a known performer within multiple government agencies.
Triple Ring translates applied science into working prototypes and advances those prototypes into commercial-ready products. This includes meeting strict regulatory requirements, developing robust supply chains, and design-for-manufacture (DFM). Equally important is our experience in successfully communicating progress and status of development projects with agency program managers in written reports and in program reviews.
— Building the right teams to win government contracts
— Navigating the proposal and funding process
— Creating plans to translate applied research into commercial success
— Executing on complex, multidisciplinary government-sponsored programs
Triple Ring has ITAR-compliant spaces and IT systems to manage Confidential Unclassified Information (CUI).
Triple Ring can flexibly work with the government and partners under various contract formats, including “other transactions,” cooperative agreements, and vendor agreements.
Our decades-long success with US government programs includes translating technologies for medical devices, diagnostics, and homeland security.
Triple Ring has delivered on programs funded by NIH, FDA, DOE, EPA, DoD, DARPA, ARPA-H, and BARDA.
Triple Ring has worked with many US R1 institutions (universities and medical centers), as well as US-based and international not-for-profit medical research institutes, and for-profit entities. Examples include the Institute for Human & Machine Cognition (IHMC), Massachusetts Institute of Technology.
Triple Ring regularly collaborates with universities, research institutes, and corporations (large and small) beginning with responses to calls and broad area announcements (BAA) and at the proposal-writing stage. We provide cost estimates, technical content, plans, and personnel to assure contract success.
Yes, we often engage after an award is made. At times project teams discover needs for additional capabilities and expertise, or changes to team structures necessitate seeking alternatives. Triple Ring is happy to pitch in when the need arises.
Triple Ring has performed both roles. Our roles are dictated by the needs of a given program.
Triple Ring does not perform classified work directly but can perform classified work through partnerships with appropriate parties. Please inquire for details.
Triple Ring has extensive expertise in developing medical devices for successful FDA approval via multiple pathways (e.g., 510(k), De Novo, PMA). We are ISO 13485 certified and have our own QMS system that clients can leverage. We author the required documents (product requirements, key hazardous situations, risk assessment) and conduct the formal design verification testing required for FDA submission. We can also advise on appropriate submission pathways.
For government programs, Triple Ring is considered a CDMO. We are licensed by the State of California’s Department of Public Health, Food and Drug Branch, to manufacture medical devices for clinical trials (clinical validation). Additionally, Triple Ring is well-connected to medical device and life science supply chains that include contract manufacturers capable of scaled production of devices.
Developing new technology is inherently difficult and risky. As a co-development company, we strive to be a trusted partner, not simply a consultant. We structure projects to meet the business needs of our clients, and we often share risk.