At iLenSys, we understand the challenges that life science companies face in turning their innovative ideas into commercial reality. We offer flexible and technical project management to ensure we can lead a product from concept through to market. We adopt a multi-disciplinary approach to life science product design, integrating knowledge of biotechnology with other skills including Mechanical, Electronics, Electrical and software design. OEMs expect more accessible, affordable design outsourcing partners to support their technology advancements at lower costs without comprise in quality and regulatory requirements, It is here iLenSys engages with Life Science Industry supporting new product development, sustaining existing products and improving the functionality.
ISO 9001
ISO 13485
Services to EPIC
ANVISA
ISO 14001
EN 46001
CE Mark
21 CFR Part 820
JGMP
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.
When you’re building complex lab instruments or analytical devices, product development can be slow, expensive, and unpredictable - especially when sensor integration is involved.
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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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This webinar will help you discover how design plays a pivotal role in minimizing parts supply risks during the development process of Analytical Instruments. Gain insights into the unique supply chain challenges that are observed in product life cycle of Analytical instruments. Learn how strategic design decisions can enhance supply chain resilience in both new & current production instruments.
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Discover how iLenSys Regulatory Master simplifies regulatory complexity and helps you manage critical components with confidence.
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Explores the development and implementation of a state-of-the-art electrical control system.
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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