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Posted by TracksNTeeth on May 28, 2024 at 7:12pm 0 Comments 0 Likes
When it comes to heavy-duty machinery like dozers, durability and efficiency are paramount. One crucial component that significantly impacts performance is the rubber tracks. In this article, we'll delve into the importance of rubber tracks for Caterpillar and Tigercat dozers, exploring how they enhance functionality and longevity.…
ContinueIZiel 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 May 13, 2020 at 5:20am — 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 May 6, 2020 at 3:47am — No Comments
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
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 March 31, 2020 at 1:03am — 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 March 23, 2020 at 2:59am — 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 March 18, 2020 at 5:39am — 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 March 12, 2020 at 2:16am — 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 March 5, 2020 at 4:29am — 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 March 5, 2020 at 4:00am — No Comments
IZiel alongwith their partners (Obelis) provide a “One-Stop Shop” to assist medical devicemanufacturers for MDD-MDR transition. IZiel ensures to focus on regulating medical devices throughout its lifecycle rather than focussing on any one stage, which is the need of MDR. The MDR seeks to address these concerns so that the end users do not face major safety or quality issues.
Added by Aniket Chaudhari on February 26, 2020 at 3:36am — 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 February 19, 2020 at 4:22am — 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 February 19, 2020 at 3:54am — No Comments
IZiel alongwith their partners (Obelis) provide a “One-Stop Shop” to assist medical devicemanufacturers for MDD-MDR transition. IZiel ensures to focus on regulating medical devices throughout its lifecycle rather than focussing on any one stage, which is the need of MDR. The MDR seeks to address these concerns so that the end users do not face major safety or quality issues.
Added by Aniket Chaudhari on February 13, 2020 at 1:14am — No Comments
IZiel alongwith their partners (Obelis) provide a “One-Stop Shop” to assist medical devicemanufacturers for MDD-MDR transition. IZiel ensures to focus on regulating medical devices throughout its lifecycle rather than focussing on any one stage, which is the need of MDR. The MDR seeks to address these concerns so that the end users do not face major safety or quality issues.
Added by Aniket Chaudhari on February 6, 2020 at 7:00am — 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 February 6, 2020 at 6:20am — No Comments
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 January 29, 2020 at 11:53pm — No Comments
IZiel alongwith their partners (Obelis) provide a “One-Stop Shop” to assist medical devicemanufacturers for MDD-MDR transition. IZiel ensures to focus on regulating medical devices throughout its lifecycle rather than focussing on any one stage, which is the need of MDR. The MDR seeks to address these concerns so that the end users do not face major safety or quality issues.
Added by Aniket Chaudhari on January 24, 2020 at 12:54am — No Comments
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