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IVDR's Summary of Safety and Performance: Your Essential GuiIVDR's Summary of Safety and Performance: Your Essential Gui

34 days ago

Delve into IVDR's Summary of Safety and Performance for crucial insights and compliance essential...

Medical Devices Registration in BangladeshMedical Devices Registration in Bangladesh

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We help you to prepare Medical Device Technical File (MDR) as per the regulatory requirement of E...

The Routes To Conformity - Navigating EU RegulationThe Routes To Conformity - Navigating EU Regulation

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Conformity Assessment Procedure for Medical Device under the Responsible Model (EU MDR 2017/745 &...

Internal Quality Audit: Key Checks for SuccessInternal Quality Audit: Key Checks for Success

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To achieve and sustain excellence, a company needs a good quality control system. We provide Inte...

Premium Organizational Management ServicesPremium Organizational Management Services

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Take a premium advantage of MAVEN's Premium Organizational Management Services. These services ar...

Annual Maintenance Contract ServicesAnnual Maintenance Contract Services

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We provide best AMC service where we take complete charge of ensuring regulatory compliance of al...

Classification of Medical Devices in VietnamClassification of Medical Devices in Vietnam

205 days ago

Medical devices in Vietnam are classified by CDSCO, Central Licensing Authority. Medical device o...

What is a Clinical Evaluation Plan and Why is it Important?What is a Clinical Evaluation Plan and Why is it Important?

218 days ago

A Clinical Evaluation Plan is a document that outlines the systematic process of assessing the sa...

Design History File for Medical DevicesDesign History File for Medical Devices

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Get your Design History File planned and approval for your medical devices in Vietnam, Malaysia, ...

Clinical Development Plan Clinical Development Plan

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A clinical development plan is a subpart of a clinical evaluation plan which aims at the devices ...

EUDAMED - European Database on Medical DevicesEUDAMED - European Database on Medical Devices

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However, the new medical devices regulations (EU MDR) contain important improvements including a ...

MHRA Registration to get UKCA MarkMHRA Registration to get UKCA Mark

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The MHRA Registration database contains manufacturer name, address, MHRA reference (account) numb...

Unraveling the relationship between EN ISO 149711 and GSPR Unraveling the relationship between EN ISO 149711 and GSPR

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The interrelationship between EN ISO 14971:2019/A11:2021 and the General Safety and Performance R...

Overall Residual Risk - How to Evaluate it ?Overall Residual Risk - How to Evaluate it ?

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The risk management standard ISO 14971:2019 is the Holy Bible for medical device risk management....

CE Mark for Medical Devices: Stay AheadCE Mark for Medical Devices: Stay Ahead

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The CE mark is of utmost importance in the European market, and understanding its intricacies is ...

European Medical Device Regulations European Medical Device Regulations

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It has been said that European Medical Device Regulations is the most significant change to the r...

Regulatory Compliance Solution CE for In Vitro Diagnostic DeRegulatory Compliance Solution CE for In Vitro Diagnostic De

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Get the EUDAMED registration done for IVD based on the regulations of EU 2017/746. We assist you ...

Medical Device Usability Testing Service providerMedical Device Usability Testing Service provider

370 days ago

We help you get done medical devices usability testing. We provide medical device usability testi...

Prepare perfect Technical File for UKCA MarkPrepare perfect Technical File for UKCA Mark

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Our consultancy helps you in establishing your products in various countries with help of our exp...

Stability Studies of Medical DevicesStability Studies of Medical Devices

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Maven helps you to design a Stability Studies of Medical Devices Plan and reduce errors. The purp...

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