Medical Device
Software Services 

RTEmd works with leading medical device, pharmaceutical, and medical software companies 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

  • 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.
  • Visit with us in RTEmd Booth #2148 at MD&M East in New York City, June 10-12, 2014 at the Jacob Javitz Convention Center. Contact us for show details or to arrange a specific meeting time.
  • Request our Device Connectivity White Paper: Avoiding Common Errors & Reducing Risk. This new white paper discusses strategies to ensure successful and sustainable connectivity performance with medical devices.