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ISO 13485 & ISO 9001 Certified

Innovation Resources

Reliability for Combination Products

As technological advances enable the merging of combination products with historically different regulatory pathways to commercialization, the need to direct attention toward the safe and reliable development of these products has emerged. Stress Engineering has the tools, expertise and reputation for designing reliability into devices, drugs and biologics as well as helping clients improve the reliability of existing products.

Medical Regulatory Support

Support for Human Factors Engineering - SES has adapted our systems and regulatory experience to include support for almost every aspect touched in the Waterfall Design Process.

Human Factors & Ergonomics

With predictive analysis and human factors testing under the same roof, our ISO 13485:2003 certified medical device development firm is rethinking user-centered design.

Cleaning Chemical Compatibility

Eliminate polymer device cracking caused by aggressive cleaning agents and disinfectants

Polymer Testing & Engineering Services

Stress Engineering’s Polymer Laboratory offers standalone testing services for many polymer characterization methods. We provide high quality test data and analytical reports at competitive rates, whether for one sample or 100 samples.

Improving the Performance of Outdoor Products

Engineering Products for your Outdoor Lifestyle - There are only a few laws that can never be broken when it comes to the development of hunting products…the laws of physics. Fortunately, Stress Outdoor® has the ability to understand and interpret the laws of physics resulting in product performance and safety advantages for our clients.

Innovations in E-Commerce Liquids Packaging

Developing Liquids Packaging Design Solutions to Eliminate E-Commerce Leakage

Pharma & Grocery Cold Chain E-Commerce Packaging

Using real-time simulation for optimized packaging solutions in pharma and grocery cold chain

Predictive Analysis at the Forefront of Medical Product Development

Predictive analysis and simulation of medical device and implant performance using nonlinear finite element analysis can significantly accelerate product development cycles while helping manufacturers to avoid costly mistakes.

Device Development Support

SES applies a Risk Management approach to the product development process that reduces cost, time-to-market, and liability risk.