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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...

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

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 ...

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

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

Classification of Medical Devices in VietnamClassification of Medical Devices in Vietnam

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

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...

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 ...

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....

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...

Trusted Biomass Pellets Export Companies in IndiaTrusted Biomass Pellets Export Companies in India

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Seeking trusted Biomass Pellets Export Companies in India? Look no further than 73 Deals! We are ...

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 ...

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...

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 ...

Du Lịch VNDu Lịch VN

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$ 100.00

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Responsibilities of a UK Responsible Person in UKResponsibilities of a UK Responsible Person in UK

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We help you find the valid UK Responsible Person who is legally placed in UK market and help you ...

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...

Medical Device Usability Testing Service providerMedical Device Usability Testing Service provider

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

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