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Posted by ramy on September 22, 2024 at 11:48pm 0 Comments 0 Likes
Posted by ramy on September 22, 2024 at 11:48pm 0 Comments 0 Likes
Posted by ramy on September 22, 2024 at 11:48pm 0 Comments 0 Likes
IZiel Healthcare provides Process Validation for Medical Devices which includes IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification), TMV (Test Method Validation) etc. Our robust Software Validation approach is aligned to IEC 62304 starting with requirements management alongwith risk management & traceability.
Added by Aniket Chaudhari on April 29, 2020 at 6:22am — No Comments
IZiel Healthcare are leading providers of engineering and regulatory services for MDD to MDR projects for medical device companies.IZiel helps you to obtain CE approvals for Class I, II & III Medical Devices, along with MDD to MDR transitions.
Added by Aniket Chaudhari on April 21, 2020 at 6:57am — No Comments
IZiel’s Onshore-Offshore Model works with 1 Onsite Member supported by a team of 3-4 engineers from our Technical Center in India. Typically, the data is collected, evaluated and evidence is developed from the process design stage throughout production. Our Model enables the company to complete the project faster and in a cost-effective manner.
Added by Aniket Chaudhari on April 14, 2020 at 7:31am — No Comments
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…
ContinueAdded by Aniket Chaudhari on April 7, 2020 at 3:27am — No Comments
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