RESI serves as the gold standard in connecting early-stage life science and healthcare companies with investors and strategic partners. As developers move forward in transforming their core technology to commercialization, we’re ready to provide the product development support they need. And to help, check out the resources below. Have questions? Need more information? Wondering if there’s a way you can speed your device to market? Let us know. We’re here to help.
DEVELOPMENT
Published Articles
A Holistic Approach To Your Medical Device’s Usability
Med Device Online – April 8, 2024
Designing for Terminal Sterilization Versus Re-Sterilization
Orthopedic Design & Technology – March 7, 2024
5 Smart Manufacturing Strategies For Medical Device Startups
Med Device Online – September 28, 2023
5 Common Startup Mistakes (and How to Avoid Them)
Medical Product Outsourcing – March 28, 2023
What’s Wrong with the Medtech R&D Department?
Med Device Online – November 22, 2022
You Have a Medical Device Proof of Concept. Now What?
Med Device Online – October 5, 2022
The 5 Common Medical Device Startup Challenges (and How to Overcome Them)
Med Device Online – June 20, 2022
REGULATORY AFFAIRS AND QUALITY ASSURANCE SERVICES
Published Articles
Key QMS Considerations For Your Medical Device Startup
Med Device Online – March 17, 2025
How to Prevent Product Misuse Through Formative Studies
Med Device Online – Dec. 9, 2024
Your 510(k) Hasn’t Sailed Through. Now What?
Med Device Online – Sept. 24, 2024
Key Considerations In “Intended Use” And “Indications For Use” Statements For Medical Devices
Med Device Online – December 14, 2023
Biocompatibility Testing Tips To Speed Your Medical Device To Market
Med Device Online – July 12, 2023
5 Key Steps For FDA Q-Submissions
Med Device Online – April 18, 2022
How to Untangle Your Medtech Regulatory, Engineering & Business Decisions
Med Device Online – January 3, 2022
Additional Resources
The Lure of the FDA Q-Sub Meeting: When (and When Not) to Call for One – Part 1
Boulder iQ Blog – March 3, 2022
The Lure of the FDA Q-Sub Meeting: When (and When Not) to Call for One – Part 2: Planning for the Meeting(s)
Boulder iQ Blog – March 27, 2023
STERILIZATION AND PACKAGING
Published Articles
Packaging for Med Device Companies: EO and CD Considerations
Medical Product Outsourcing – Oct. 22, 2024
Medical Device Assembling And Packaging: Should You Outsource?
Medical Product Outsourcing – June 18, 2024
Medical Device Packaging Labels
Med Device Online – March 16, 2022
Additional Resources
Rapid Prototyping Materials: Are They Compatible With EO Sterilization?
Boulder iQ Blog – January 29, 2023
Chlorine Dioxide Sterilization for Medical Devices: Benefits
Chlorine Dioxide Sterilization: A Green, Environmentally Conscious Option