Medical Device
Software Services 

Providing compliant software development and quality/regulatory services to medical device and pharmaceutical clients to:


New Product Design & Development
Sustaining Engineering
Quality & Regulatory

ISO 13485 and ISO 9001 certified QMS, IEC 62304 compliant

“RTEmd understood our goals and executed flawlessly—from requirements definition through system verification & validation.”

What’s New

  • Request our new white paper: Sustaining Engineering Best Practices. This white paper examines how effective sustaining engineering practices can extend the life and value of deployed medical products while delivering innovation to users.
  • Follow a standards based, compliant process to produce medical devices more quickly, to speed regulatory approvals, and to produce output which matches desired inputs. Get our new white paper to learn how.
  • RTEmd expands breadth of experience with infusion pump and diabetes device projects. Contact us for additional details.