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ISO 13485 & ISO 9001 Certified

Innovation Resources

Reducing the Cost of HPP Package Development

Until now, High Pressure Processing (HPP) package development has relied exclusively on an iterative process of prototyping and package testing, both of which are expensive and time consuming. Stress Engineering developed a new technology to accelerate development and reduce costs via the application of predictive computational methods, frequently referred to as ‘insilico’ performance simulation testing.

Pharmaceutical Design Analysis and Testing Services

Process Engineering
Mechanical Integrity
Facilities
Manufacturing Support
Combination Products
Pharmaceutical Packaging

Medical Devices Overview

Design & Analysis
Failure Analysis
Testing
Materials
Reliability
Manufacturing Support
Packaging

Drug Delivery Case Studies

Wearable Drug Delivery System Reliability Planning
Injection Pen Design for Manufacturability
Inhaler Design & Simulation
Test Fixture & Equipment Development

Drug Delivery System Experience

Failure Investigations, Design Support, Manufacturing Support, Testing, Syringes - Prefilled & Unfilled

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.

Human Factors & Ergonomics

With predictive analysis and human factors testing under the same roof, our ISO 13485:2016 certified medical device development firm is rethinking user-centered design.

Cleaning Chemical Compatibility

Eliminate polymer device cracking caused by aggressive cleaning agents and disinfectants

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.