Blog Posts

Top Careers in Pharmacy

Posted by Poddar College on September 19, 2024 at 12:34am 0 Comments

Pursuing a career in Pharmacy, either in India or abroad entails large career opportunities for all medical students. The demand for professional pharmacists is constantly increasing, and owing to this, they can work in different areas of employment like Pharmaceutical Industries or Hospital Pharmacies.

Poddar International College, one of the best College in Jaipur provides courses in Pharmacy along with other courses.

Pharmaceutical Industries

Pursuing a career in Pharmacy,…

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Highlight on Girl Wedding Photographers: Experiences of Love and Perseverance

Posted by BABU on September 19, 2024 at 12:28am 0 Comments

The marriage images business has observed a significant rise in the amount of woman photographers. This development is reshaping the industry and providing couples a varied selection of views and models for acquiring their particular day. Girl wedding photographers bring unique sensibilities and a definite Female Wedding Photographer to their work, usually focusing the emotional and intimate aspects of the event. Their existence in… Continue

How Peering Exchanges Work: A Behind-the-Scenes Look at Internet Traffic Flow

Posted by DE-CIX India Internet Exchange on September 19, 2024 at 12:26am 0 Comments

The internet is an intricate network of data flowing across the globe. But how exactly does that traffic get from one network to another? This process largely depends on peering exchanges, the unseen hubs that enable networks to efficiently share traffic. In this article, we'll explore what a peering exchange is, how it works, and its importance, particularly in…

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Cara Centang Hijau di WhatsApp (10 Langkah) No Ribet!

Posted by Lovina Lindy on September 19, 2024 at 12:07am 0 Comments

WhatsApp merupakan media sosial dengan jumlah pengguna terbanyak di dunia. Kamu akan selalu menggunakannya untuk komunikasi setiap hari. Bahkan, sejumlah pihak memanfaatkannya sebagai ladang cuan dan menarik perhatian konsumen dengan lencana verifikasi hijau. Cara centang hijau di WhatsApp pun sangat mudah lho.

Selengkapnya https://www.dumados.com/2024/09/cara-centang-hijau-di-whatsapp-10.html

Aniket Chaudhari's Blog – September 2021 Archive (19)

Regulatory Remediation Services

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) and resolve queries, if any, from USFDA.

read more@…

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Added by Aniket Chaudhari on September 28, 2021 at 1:09am — No Comments

Remediation for Medical Devices

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.

Read more@…

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Added by Aniket Chaudhari on September 28, 2021 at 1:08am — No Comments

Remediation for Medical Devices

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.

Read more@…

Continue

Added by Aniket Chaudhari on September 27, 2021 at 8:04am — No Comments

FDA Remediation Consultants

Remediation Consultants at IZiel implement best practices in Design-Development Process and Quality Management Systems ensuring effective and timely deliveries. IZiel provides expert solutions to remediate 483 observations and warning letters. IZiel teamworks with medical device companies across the globe to achieve regulatory andstandard compliance.

Read more@ https://iziel.com/fda-remediation-consultants/

Added by Aniket Chaudhari on September 27, 2021 at 8:02am — No Comments

MDD to MDR Part 2- How you help yourself –How consultant can support you

As old manufacturer of medical device you were naturally MDD compliant and to remain in business you will have to become MDR compliant too.

As Medical device business you also must have accounted the compliance cost to your product to assess the product cost and added your profitability to arrive at Product cost. The same exercise is now necessary as compliance cost…

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Added by Aniket Chaudhari on September 22, 2021 at 6:30am — No Comments

USFDA Consulting Firms

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…

Continue

Added by Aniket Chaudhari on September 20, 2021 at 6:33am — No Comments

FDA Remediation Consultants

Remediation Consultants at IZiel implement best practices in Design-Development Process and Quality Management Systems ensuring effective and timely deliveries. IZiel provides expert solutions to remediate 483 observations and warning letters. IZiel teamworks with medical device companies across the globe to achieve regulatory andstandard compliance.

Read more@ https://iziel.com/fda-remediation-consultants/

Added by Aniket Chaudhari on September 20, 2021 at 5:52am — No Comments

USFDA Consulting Firms

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…

Continue

Added by Aniket Chaudhari on September 20, 2021 at 5:52am — No Comments

USFDA Consultants Medical Device

Medical Device Manufacturers require USFDA Approvals to sell their products in USA. USFDA differentiates product approvals in Class I, II &III depending upon the risk associated. The submissions include self-certification, 510(k) and PMA depending upon the class of the product.IZiel implements an Outcome-Based Delivery Model to provide complete solution from developing engineering documentation to receiving USFDA Approvals & establishment registrations thereafter. Our teams from USA…

Continue

Added by Aniket Chaudhari on September 15, 2021 at 1:26am — No Comments

MDD to MDR

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.

Read more@ https://iziel.com/mdd-to-mdr/

Added by Aniket Chaudhari on September 15, 2021 at 1:26am — No Comments

Form 483 Compliance

IZiel provides expert solutions to remediate FDA 483 observations and warning letters. IZiel team works with medical device companies across the globe to achieve regulatory and standard compliances. We take great pride in implementing best practices in Design-Development Process and Quality Management Systems ensuring effective and timely deliveries.

Read more@ https://iziel.com/form-483-compliance/

Added by Aniket Chaudhari on September 15, 2021 at 1:15am — No Comments

USFDA Regulatory Consultants

IZiel helps you to obtain US FDA and CE approvals for Class I, II & III Medical Devices. Our Regulatory Consultants in US, Europe and India have thorough knowledge of USFDA & MDR Requirements alongwith extensive experience in submissions and approvals. IZiel works with the company to develop comprehensive documents in compliance with the regulatory requirements.

Read more@ https://iziel.com/regulatory-remediation/

Added by Aniket Chaudhari on September 15, 2021 at 1:14am — No Comments

USFDA Consultants Medical Device

Medical Device Manufacturers require USFDA Approvals to sell their products in USA. USFDA differentiates product approvals in Class I, II &III depending upon the risk associated. The submissions include self-certification, 510(k) and PMA depending upon the class of the product.IZiel implements an Outcome-Based Delivery Model to provide complete solution from developing engineering documentation to receiving USFDA Approvals & establishment registrations thereafter. Our teams from USA…

Continue

Added by Aniket Chaudhari on September 9, 2021 at 6:50am — No Comments

MDD to MDR

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.

Read more@ https://iziel.com/mdd-to-mdr/

Added by Aniket Chaudhari on September 9, 2021 at 6:49am — No Comments

Form 483 Compliance

IZiel provides expert solutions to remediate FDA 483 observations and warning letters. IZiel team works with medical device companies across the globe to achieve regulatory and standard compliances. We take great pride in implementing best practices in Design-Development Process and Quality Management Systems ensuring effective and timely deliveries.

Read more@ https://iziel.com/form-483-compliance/

Added by Aniket Chaudhari on September 9, 2021 at 6:27am — No Comments

USFDA Regulatory Consultants

IZiel helps you to obtain US FDA and CE approvals for Class I, II & III Medical Devices. Our Regulatory Consultants in US, Europe and India have thorough knowledge of USFDA & MDR Requirements alongwith extensive experience in submissions and approvals. IZiel works with the company to develop comprehensive documents in compliance with the regulatory requirements.

Read more@ https://iziel.com/regulatory-remediation/

Added by Aniket Chaudhari on September 9, 2021 at 6:26am — No Comments

Remediation for Medical Devices

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.

Read more@…

Continue

Added by Aniket Chaudhari on September 1, 2021 at 7:26am — No Comments

Form 483 Compliance

IZiel provides expert solutions to remediate FDA 483 observations and warning letters. IZiel team works with medical device companies across the globe to achieve regulatory and standard compliances. We take great pride in implementing best practices in Design-Development Process and Quality Management Systems ensuring effective and timely deliveries.

Read more@ https://iziel.com/form-483-compliance/

Added by Aniket Chaudhari on September 1, 2021 at 7:11am — No Comments

USFDA Regulatory Consultants

IZiel helps you to obtain US FDA and CE approvals for Class I, II & III Medical Devices. Our Regulatory Consultants in US, Europe and India have thorough knowledge of USFDA & MDR Requirements alongwith extensive experience in submissions and approvals. IZiel works with the company to develop comprehensive documents in compliance with the regulatory requirements.

Read more@ https://iziel.com/regulatory-remediation/

Added by Aniket Chaudhari on September 1, 2021 at 6:25am — No Comments

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