|Products and Services:||2,201|
|Articles and publications:||11,536 (+5)|
|Tenders & Vacancies:||12|
|Phone||+1 (585) 383-1290|
|Fax||+1 (585) 383-1294|
|Contact person||Bob Ruppenthal, President|
Over 90% of our medical device customers return to engage us in additional software outsourcing opportunities…new product development, sustaining engineering and quality/regulatory support.
Experts at improving time-to-market, reducing liability risks, reducing manufacturing/service costs, RTEmd has a portfolio of services covering the entire software lifecycle for complex medical equipment.
ISO 13485 & ISO 9001 certified, with extensive clinical and FDA experience, RTEmd takes a disciplined approach to everything we do. With a thorough understanding of technical requirements, business goals and quality/regulatory standards, we have a proven track record at improving our clients’ business performance.
RTEmd has over 30 years of successful experience with: in vitro diagnostics, medical imaging, patient monitoring, surgical applications, laboratory equipment, ophthalmology, nephrology and therapeutics.
Please contact us at PH 585.383.1290 or visit us at www.rtemd.com to learn more about our software outsourcing services including:
New Product Development-Requirements analysis, design, code construction, testing, documentation & agency submittal…from concept to deployment, we fulfill exact requirements with software done right the first time.
Sustaining Engineering- Resolve in-field issues, add new functionality, adapt to regulations, reduce manufacturing costs, and solve obsolescence issues… from deployment to end-of-life, we extend the revenue of your current products.
Quality & Regulatory Support- Comprehensive SQA services, DHF documentation, compliance gap analysis & remediation, verification planning & test execution, validation expertise, support for agency submission.. throughout the lifecycle, we reduce your risk and help ensure compliance