Medical Instrumentation
Embedded systems have greatly influenced the evolution of medical instruments, making computerization and miniaturization possible. The use of embedded systems in these devices has metamorphosed these instruments into smarter, portable, and network enabled devices with sophisticated diagnostic capabilities, delivering high precision and accuracy. The integration of wireless technology with medical devices has enabled the use of mobile devices for remote health monitoring, benefiting healthcare workers by reducing “time-to-care”.
As the functionality of these applications increases because of embedded hardware, medical devices increasingly rely on complex embedded software. The challenge of bringing cutting-edge devices to market is compounded by the need to ensure patient safety as well as meet regulations from agencies such as the Food and Drug Administration (FDA).
Persistent has demonstrated expertise in medical product quality processes and product certification standards. This helps medical device manufacturers accelerate business in the market space by producing high quality productswith minimal development time.
The Persistent Medical Instrumentation team has extensive experience with the following regulatory and medical quality process standards:
- HIPAA, HL7, DICOM
- ISO13485
- FDA, CFR 21 Part 11, IQ, OQ, PV, GMP, LG
PersistentOfferings
Persistent Advantage
- Partnering with Persistent allows customers to revive and re-launch legacy products with industry-standards and up-to-date features
- Reduced time to market equips customers with a competitive edge and the ability to roll out more products
- In depth embedded product development domain expertise acquired through years of customer engagements
- Leveraging Persistent’s extensive development and test resources leads to significant cost savings