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We offer specialized services to physicians, start-up biotech and medical device companies specializing in cell and tissue-based products.

(970) 658-0817
contact@dremedtech.com
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Biotech/Med Device

Proof-of-Concept

Our company structure is designed to offer consulting and bench/laboratory resources as a package. Our aim is to offer guidance in your scientific approach (consulting) and execute affordable, high impact experiments to produce the metrics your company requires while keeping budgets and sensitive timelines in mind. This work is often essential in the seed/angel fundraising phases of companies that require the measurement/quantification of key output metrics to ensure viability of their start-up.
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Data Collection from End-Users

If you have a commercialized product and are seeking assistance in gathering data from your physician network for marketing or publication purposes, we will work with your team to maximize the integrity and power of your data. We will be integrated in the process to successfully establish the packaging/shipping logistics and the appropriate data-endpoints/metrics to ensure the utility of your data for your intended purpose. Refer to our “Physicians” tab for more information and contact us when you are ready for more information!

Intellectual Property

Your aim may be to generate experiments that result in IP in while in the PoCphase of your product or, in later phases as adaptations are made to your product. We pride ourselvesin assisting you throughout consulting and research services via the development and completion of experimental designs and results that highlight the novelty of your product compared to what exists in the market as well as ancillary improvements in latter generations of your product over the predecessors. If you have a specific experiment already designed and simply need the execution of the protocol, we are happy to perform this service as well!

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Commercialization

Depending on your device or tissue, you have determined your regulatory pathway via collaboration with the appropriate advisors/consultants based on your device outputs and/or claims. At this phase, it is essential to collect data to submit to the FDA for review and potential approval of your product. We are here to consult and perform the bench work necessary to produce compelling and convincing data that supports your application while working closely with the regulatory consultancy you have selected.