Academic institutions and both large and small companies can leverage government funding to get their advanced technologies to market. Triple Ring is a proven performer with multiple agencies and an experienced development partner in translating early-stage technologies into commercial-ready products. With deep technical capabilities and extensive experience, Triple Ring is an ideal teaming partner for academics and companies working with the government to develop their technologies and products.
Triple Ring’s team translates applied science into working prototypes and working prototypes into commercial-ready products. This includes supply-chain considerations in development and design-for-manufacturing, as well as meeting regulatory requirements (e.g., FDA approval, UL and CE approval, and others). Equally important is our experience in successfully communicating progress and status of development with agency program managers, in written reports, and in program reviews.
— Building the right teams to win government funding
— Navigating the proposal and funding process
— Developing a plan to translate applied research into commercial success
— Executing on complex, multidisciplinary government-sponsored programs
Triple Ring has ITAR-compliant spaces and systems 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.
We have worked with a number of government agencies either directly or indirectly through our teaming partners.
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.
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.