Our Electrical Engineering Skillsets
Our team has a wealth of experience in designing electro-mechanical devices, connected devices and test equipment. We excel at all the stages of product development from customer engagement, planning and requirements gathering to handover and post-handover support including concept development and design strategy, prototyping and design realization, and design iteration and enhancement.
Electro-mechanical and connected medical devices improve patient experience and quality of care. Therefore, NEUMA partners with its customers to get products to market quickly and successfully. Through a Design for Production (DFP) approach we focus on producing innovative solutions created with the foresight of commercial scale to avoid the delays that plague many programs as they move from prototype to high volume production.
NEUMA's electrical engineers offer:
Understanding and definition of critical customer requirements, timelines and deliverables, requirements traceability to system requirements, capture of specific usability requirements for User Interface (UI) components, preliminary component selection and technology approach, and consideration of external requirements such as regulatory (FDA, CE) and international electrical safety standards applicable to the type of device being designed.Explore More
At NEUMA, you'll find experts who can help with:
Hardware specifications generation detailing expected design performance criteria, impact analysis of component selection on supply chain (long lead time parts, end-of-life considerations, analog and digital circuit design (including widely-used microcontrollers such as the STM8 and MAXIM 32660 (Cortex-M4) based devices), rapid Arduino prototyping of digital control circuits, and bus technologies including GPIO, SPI, I2C, async serial communication.Explore More
We offer expertise with:
Motor control (stepper, servo and brushed/brushless motors), low power (battery-operated) wearable technologies, UI technologies (displays, keypads, switches, annunciators), sensor interface/integration including magnetic proximity and optical detection technologies, through hole, surface mount and multilayer printed circuit board topologies, high density PCB layout, circuit behavior prediction from design inputs including system, electrical, regulatory and safety requirements, and schematic capture and PCB layout using Altium Designer, our preferred PCB design tool, first article bring-up and evaluation and hardware integration with firmware, and programming/testing PCBAs.Explore More
NEUMA can help when you need:
A board manufacturer liaison to resolve issues, electrical safety testing (ETL) support to applicable standards in conjunction with a 3rd party test body, test reports to support regulatory submissions, component selection, tolerance analysis and component end-of-life review, Failure Mode Effect Analysis (FMEA) based on the electrical design, risk analysis and risk management planning associated with electrical design tasks, hardware and firmware debugging and incremental design change to address specific areas where specifications are not met, data collection from operational prototypes, contract manufacturer liaison service for design transition to production.Explore More
Meet our Electrical Engineering Experts
PRINCIPAL ELECTRICAL ENGINEER
Markets That Benefit from Our Electrical Engineering Solutions
Our experts understand the interaction between devices and drug products. Our experience includes injectables, nasal, respiratory, and more.
Biologics & Cell and Gene Therapy Services
We understand why “the product is the process” and how to implement solutions to your unique challenges.
Drug development is constantly evolving with new regulations and technology. We stay up to date to maintain your compliance.
The NEUMA Electrical Engineering Difference
NEUMA offers a forward-thinking approach to the product development lifecycle, accessing both industry-leading technologies and disruptive innovations to position products for commercial success.
Our team applies Kymanox’s development toolkit of project management, development, and quality management tools that can be customized to the needs of your company and project to ensure efficient and “fit for purpose” solutions to meet your project objectives.
Our team's broad experience and integrated development approach ensure the Right First Time products for unmet patient needs in accordance with US FDA, EU EMA, and rest-of-world regulatory requirements.
We offer unmatched experience and knowledge across pharmaceuticals, biologics, medical devices, combination products, and "in vitro" diagnostics, so we are equipped to tackle any project in these areas. Our Development leads serve as a central hub to leverage subject matter experts from across the organization.
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