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Blog Posts
Medical Device Software Validation
Posted by Aniket Chaudhari on April 27, 2024 at 4:35am 0 Comments 0 Likes
IZiel has highly trained software engineers with multiple years of experience in software coding, software verification and software validation. The team consists of senior engineers who have worked in design and development of highly sophisticated implantable devices at industry leading companies, with direct expertise in software V&V. This team, with the support of IZiel’s regulatory and clinical experts, are decidedly equipped to handle complex software validation activities for…
ContinueRemediation for Medical Devices
Posted by Aniket Chaudhari on April 27, 2024 at 4:35am 0 Comments 0 Likes
IZiel team in collaboration with the customer utilize an extensive & comprehensive methodology to complete the remediation project. Our Onshore-Offshore Model with strong project management ensure deliveries with faster timelines, flexible resources and in cost-effective manner.IZiel utilizes the best practices in design and development while ensuring compliance with regulation to ensure a speedy and compliant design and development process.
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Continuedsadsd
Posted by PP on April 27, 2024 at 4:34am 0 Comments 0 Likes
USFDA Consulting Firms
Posted by Aniket Chaudhari on April 27, 2024 at 4:34am 0 Comments 0 Likes
IZiel adopts an analytical mindset thus enabling us to root out all possible non-conformances in a regulatory submission. IZiel works in collaboration with your team to develop the complete Design History File (DHF) including requirements management, risk management, process validations and software validations using robust design controls process and quality system procedures. Thereafter, IZiel team works with their regulatory team in USA to complete the submissions (510k or PMA) for USFDA…
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