We offer high quality FEA and design validation services to test and optimize products on a virtual environment before being developed and manufactured. It could be from the general finite element models to fully customized simulation solutions, our team is able to tackle and offer solutions, improvements in design for real time engineering challenges of your products in a timely and cost efficient manner.
iLenSys offers services regarding hand calculation of engineered structures, in order to carry out the structural analysis, design and code checking of structures comply with ASTM, DNV, ASME, API, EN, as well as other industry standards and design codes. Finite element analysis and combines these results with the relevant code checks, by ensuring a reliable practice to deliver a solution able to meet the highest industry standards.
The "News & Updates" section features the latest developments and innovations in our services and solutions, including engineering services, product compliance, environmental regulations, Obsolescence Management, and regulatory & product safety.
Product development teams today face far more than just obsolete components. While EOL-End of Life parts often receive the most attention, manufacturers are increasingly affected by supply shortages, regulatory changes, lifecycle uncertainty, and sourcing risks that can disrupt production, delay product launches, and increase engineering costs.
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Why Automation Equipment OEMs Must Treat Obsolescence Management as a Core Business Process—Not an Engineering Afterthought
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How leading organizations are shifting from reactive compliance to proactive regulatory management
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Discover how iLenSys Regulatory Master simplifies regulatory complexity and helps you manage critical components with confidence.
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A leading analytical instrument OEM was manufacturing current-generation laboratory instruments used in high-precision testing and measurement environments.
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We highlight the mandatory implementation of EUDAMED (European Database on Medical Devices) and what it means for manufacturers operating under the EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR).
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iLenSys Technologies Pvt. Ltd.
8-2-293/82/L/231/ABC,
MLA Colony, Road No: 12, Banjara Hills,
Hyderabad, Telangana 500 034
Phone: 040 – 66998246, 040 – 66998234
Email: info@ilensys.com