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As more and more medical devices and lab instruments are becoming dependent on embedded and associated software, the new medical software development standards come into force. Innovative & reliable software are fast becoming the differentiator for manufacturers of medical devices and lab automation instruments. OPTRA's extensive experience in the LifeScience and HealthCare arena, combined with regulatory knowhow, domain expertise with software engineering skills and an innovative global delivery model, enables you to minimize time and costs, thus ensuring that you get more with less. OPTRA strictly abides by ISO 9001, CMM Level 3 Quality, ITIL, TL9000, BS 15000, and Six Sigma process quality standards and uses standardized release processes.
Optra's Expertise
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In-Vitro Diagnostics |
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Microarrays / NextGen Systems |
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Patient Monitoring Systems |
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Sequencing Systems |
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Clinical Imaging Systems |
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High Content Cell Screening Systems |
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Therapeutic Devices |
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Digital Microscopy / Pathology / Toxicology Systems |
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Mass Spec / Chromatography Systems |
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Gel Electrophoresis Systems |
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FCS / Single Cell Systems |
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Why partner with OPTRA?
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Extensive experience exclusively serving Medical Devices and Lab automation market. |
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An in-house team of software professionals, scientists, medical doctors and regulatory experts. |
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“Work-for-Hire” option facilitating you to own code and IPR. |
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Ready building blocks resulting into quicker delivery helping you reduce time to market. |
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50% costs with 100% quality and 200% enhanced SDLC leveraging Global Delivery Model. |
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