Welcome to TEM BioMed, LLC
Strategic Device Consulting, Preclinical Study Planning
- Preclinical Study Design
- In Vivo Testing
- FDA Research
- GLP Study Director
- Medical Device Safety Strategy
- Biocompatibility Support
- Preclinical Study Design
- In Vivo Testing
- FDA Research
- GLP Study Oversight
- Medical Device Safety Strategy
- Biocompatibility Support
Preclinical Study Design
Clarity Before the Study Begins
Better study decisions start before the protocol is final.
Preclinical studies are too important to approach with a generic testing plan. We work with sponsors, startups, laboratories, and development teams to shape customized studies around the product, the regulatory path, the model, and the evidence needed to move forward with confidence.
Getting experienced guidance before testing decisions are finalized helps teams make smarter study decisions with greater clarity and confidence.
WHY TEM BIOMED
Focused Expertise and Clear Guidance for Complex Preclinical Work
Focused Expertise and Clear Guidance for Complex Preclinical Work
A strong preclinical plan is more than a checklist. The right study strategy can save time, reduce testing costs, and lead to more meaningful data from the start.
We will guide you through GLP study goals, biological evaluation plans, ISO 10993 testing strategy, and the broader development path.
- Strategic research before study design
- Product-specific guidance
- Specialized study planning
- Biological safety considerations
- Clear communication and organized reporting
Our PROCESS
A simple process for moving from product questions to a study-ready path
1
Understand the Product
2
Define the Evidence Needed
3
Select the Right Model
4
Build the Study Plan
5
Support Study Execution
6
Tell the Data’s Story
ABOUT THADD
Led by Thaddeus Williams, DVM
Experienced preclinical guidance from someone who understands how studies move from idea to execution to usable data.
Thaddeus Williams brings hands-on experience in preclinical research, in-vivo study design, GLP Study Direction, and medical product development. Through TEM Biomed, he supports teams that need thoughtful study planning and scientific oversight, and practical guidance across the nonclinical path.
CORE SERVICES
Preclinical Guidance Where the Details Matter
Focused support for the planning, oversight, and interpretation work that can shape the success of a study.
- Preclinical Study Design
- Medical Device Product Development Strategy
- Biological Evaluation of Medical Devices
- GLP & Nonclinical Study Oversight
- CRO / Vendor Selection Support
- Report Review & Regulatory Readiness
WHO TEM BIOMED HELPS
Built for Teams Moving Toward the Next Milestone
Support for teams that need experienced preclinical thinking before the next major decision.
Medical Device & Biotech Sponsors
Startups & Emerging Companies
This is really good: “Smart study decisions early, before budget is committed in the wrong direction.”
Labs & CRO Teams
Skilled study direction, protocol input, oversight, or scientific interpretation.
Contact Us
Have a Product, Study, or Testing Question?
Share where you are in development and where you need support. TEM Biomed will help you identify the next right step.