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電子煙5000口可以抽多久?

Posted by dajksdhj21 on September 19, 2024 at 10:23pm 0 Comments

電子煙的使用時間取決於多種因素,包括吸煙頻率、每口吸入的量以及設備的電池壽命等。一般來說,5000口的電子煙可以使用數天到數周,具體時間因人而異。如果您每天吸200口,那麼5000口大約可以使用25天。







電子菸5000口可以抽多久?







電子煙的使用時間主要取決於您每天吸煙的頻率。例如,如果您每天吸200口,那麼5000口的電子煙可以使用約25天(5000口 ÷ 200口/天 =…

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電子煙40mg是多少尼古丁?

Posted by dajksdhj21 on September 19, 2024 at 10:22pm 0 Comments

電子煙煙液的尼古丁含量通常以每毫升(mg/ml)為單位表示。40mg的尼古丁含量意味著每毫升電子煙液中含有40毫克的尼古丁。為了更好地理解這個概念,我們可以將其與傳統香煙進行比較。

傳統香煙與電子菸的尼古丁含量比較

一根普通香煙大約含有12毫克的尼古丁,但在吸煙過程中,人體實際攝入的尼古丁量約為1-2毫克。因此,如果您每天吸20根香煙,您實際攝入的尼古丁大約是20-40毫克。

溫馨提示:購買時及時聯繫電子煙專賣店客服反饋,以確保買到喜歡的口味和安全使用電子煙。

電子煙…

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飛機上可以帶電子煙嗎?

Posted by dajksdhj21 on September 19, 2024 at 10:09pm 0 Comments

飛機上可以攜帶電子煙,電子煙及其配件(尤其是包含鋰電池的部分)不能放在託運行李中,而必須隨身攜帶。以下是一些關鍵原因和相關規定:







🟢禁止託運的原因



鋰電池風險:電子菸通常包含鋰離子電池,這種電池在某些情況下可能會過熱、起火甚至爆炸。將鋰電池放在託運行李中,如果發生問題,機組人員無法及時處理,因此航空公司通常要求將其放在隨身行李中,以便在緊急情況下能夠迅速應對。



國際航空運輸協會(IATA)規定:根據IATA的危險品規定,鋰電池應隨身攜帶,而不是託運。這些規定旨在確保飛行安全,航空公司通常會嚴格遵守這些規定。



🟢具體規定…

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Stepping into the Future: The Role of Technology in Footwear Evolution

Posted by freeamfva on September 19, 2024 at 9:31pm 0 Comments

Stepping into the Future: The Role of Technology in Footwear Evolution



Footwear has come a long way from its humble beginnings as a basic necessity for protecting our feet. Today, technology plays a pivotal role in the evolution of footwear, driving innovation and transforming the industry. This article explores how technological advancements have revolutionized footwear design, production, and functionality, making shoes more than just a fashion statement.



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Aniket Chaudhari's Blog – July 2022 Archive (19)

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…

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Added by Aniket Chaudhari on July 18, 2022 at 8:27am — 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 July 18, 2022 at 8:27am — No Comments

Medical Device Software Validation

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…

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Added by Aniket Chaudhari on July 18, 2022 at 8:26am — 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 July 18, 2022 at 8:26am — No Comments

Document review services New Jersey

A Document Review Company is engaged in reviewing the documents in eDiscovery stage of a litigation. A few document review companies provide technology based solutions in collection and review of documents through an automation process. However, SKJ Juris is a document review company that firmly believes in human interface/ intervention, as an essential element in reviewing the documents which can be initially segregated by a solution through automation but is mandatorily required to avoid…

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Added by Aniket Chaudhari on July 12, 2022 at 6:28am — No Comments

Document review services Ohio

A Document Review Company is engaged in reviewing the documents in eDiscovery stage of a litigation. A few document review companies provide technology based solutions in collection and review of documents through an automation process. However, SKJ Juris is a document review company that firmly believes in human interface/ intervention, as an essential element in reviewing the documents which can be initially segregated by a solution through automation but is mandatorily required to avoid…

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Added by Aniket Chaudhari on July 12, 2022 at 6:28am — No Comments

MDD to MDR Consultant

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.

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

Added by Aniket Chaudhari on July 12, 2022 at 4:47am — No Comments

MDR Consultants

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.

Read more@ https://iziel.com/mdr-consultants/

Added by Aniket Chaudhari on July 12, 2022 at 4:47am — No Comments

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 July 12, 2022 at 3:46am — 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.

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

Added by Aniket Chaudhari on July 12, 2022 at 3:45am — No Comments

Form 483 Remediation

Medical device manufacturers receive observations (Form 483) and / or warning letters on completion of USFDA Audit. The document outlines any violations of Good Manufacturing Practices (GMP’s) such as the facility, equipment, processes, controls, products, employee practices or records.IZiel has successfully assisted medical device companies to resolve these observations with efficiency and accuracy.

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Added by Aniket Chaudhari on July 12, 2022 at 3:35am — 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…

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Added by Aniket Chaudhari on July 12, 2022 at 3:32am — No Comments

MDD to MDR Consultant

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.

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

Added by Aniket Chaudhari on July 12, 2022 at 3:31am — No Comments

IQ OQ PQ Medical Devices

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.

Read more@ https://iziel.com/what-is-iq-oq-pq-medical-devices/

Added by Aniket Chaudhari on July 12, 2022 at 3:31am — 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 July 12, 2022 at 3:30am — 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 July 7, 2022 at 6:19am — No Comments

Medical Device Software Validation

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…

Continue

Added by Aniket Chaudhari on July 7, 2022 at 6:18am — 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 July 7, 2022 at 6:18am — 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 July 7, 2022 at 6:18am — No Comments

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