Advisory Services

Our consulting services help you navigate the complex preclinical space and walk you through the steps it takes to move your unique idea from ideation or prototype to a regulatory approved product.  Whether you are experienced in this industry or you are preparing to test your company’s first product, we look forward to helping you prove your ideas.


Your project will benefit from both our business team’s 20 plus years of life science development and management expertise as well as our scientific team’s wealth of technical knowledge on testing requirements and best practices.


TriMetis will not only support you in all preclinical stages but can assess your company’s critical concerns and opportunities; from strategy, marketing, organization, operations, technology, transformation, digital, advanced analytics, mergers & acquisitions and sustainability across all biotech industries and geographies.

Begin putting your ideas in motion by contacting us here

Launch Your Product

Moving your product from ideation to launch can be a daunting process, but we are here to help.

Accelerate your product’s development and avoid pitfalls by leveraging TriMetis’ expertise and decades of experience commercializing products through the preclinical and clinical phases of development. Through extensive business plan development, strategy (including marketing and selling), budgeting and contracting experience we can prepare you for the steps to come.

Contact us here for more information and to conduct a comprehensive risk assessment to determine which of these tests need to be performed on your unique product. We offer this service for free if you continue in partnership with our team for the recommended testing protocols.

Regulatory Services

We can work with you to determine what tests are needed to move your product’s development forward. TriMetis seamlessly partners with MRC|X to provide our clients with regulatory assessment, planning and the preparation of submissions and filings for both the US and EU markets.


Combined, MRC|X has over 35 years of experience in the life science space, specializing in the medical device, biologics, and tissue fields. Their team focuses on comprehensive solutions for regulatory, quality assurances, clinical consulting, and adhering to compliance services.

10993 Consulting

The U.S. Food and Drug Administration and international regulatory bodies alike (China Food and Drug Administration (CFDA), EU Notified Bodies, etc.), call for medical devices to be tested in accordance with the International Organization for Standardization (ISO) 10993 guidelines which determine the product’s potential toxicity.


To learn more about our full-range testing biocompatibility services click here (link to medical device page).

To get started on your free risk assessment